April 3, 2014


Retail Level: Recall



Product:Demerol™
Moore's Re-order#: 10313
Lot #:221303A

NDC# 00409120301

Manufacturer:McKesson/Hospira

PRODUCT SUBJECT TO RECALL

Moore Medical LLC received the following recall from McKesson/Hopsira. Hospira, Inc is voluntarily recalling the above listed item due to a customer complaint of a missing primary label on an ampul. Medical questions can be directed to Hospira Medical Communications at the following number – 800-615-0187. Affected product started shipping February 2013 to present.

Please check your inventory for the above product and lot number. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


April 3, 2014


Retail Level Recall



Product:Monsels Solution
Moore's Re-order#: 87199
Lot #:1292-00, 1368-00, 1595-00

Manufacturer:Medical Chemical Corp (MCC)

PRODUCT SUBJECT TO RECALL

Moore Medical LLC received the following recall from Medical Chemical Corp (MCC).

Medical Chemical Corp (MCC) is issuing a voluntary product recall for Monsel’s Solution 5548E-2oz - Lot Number 1292-00, 1368-00, 1595-00. A number of complaints have been received stating that these lots have a precipitate (to separate from solution).

Medical Chemical Corp has determined that there is no threat to either the health or safety of persons regarding the use of this product according to the label directions. This has been traced to one lot of source material.

Furthermore, this issue has been resolved by using an alternate source for the raw material and we are continuing the manufacture of this product with new approved material. Please return affected product to Moore Medical for credit.

Affected product was shipped January 2013 to present. Please check your inventory for the above product and lot number. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


April 3, 2014


Retail Level Recall



Product:Indomethacin Caps
Moore's Re-order#: 17946
Lot #:TE32134

NDC 00093402901

Manufacturer:Mckesson/Teva Pharmaceuticals USA, Inc

PRODUCT SUBJECT TO RECALL

Teva Pharmaceuticals USA, Inc is voluntarily recalling the above item/lot because the laboratory investigation was not performed in accordance with strict adherence to the FDA Guidance for Industry Investigating Out-of Specification Test Results for Pharmaceutical Production. Affected product started shipping April 4, 2013.

Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


March 24, 2014


Retail Level Recall



Product:Qvar Inhalation Aerosol with Adapater
Moore's Re-order#: 96535
Lot #:120088

NDC 59310020240

Manufacturer:McKesson/Teva Pharma

PRODUCT SUBJECT TO RECALL

Moore Medical LLC received the following recall from McKesson/Teva Pharmaceuticals USA, Inc.

McKesson /Teva is voluntarily recalling QVAR INHAL AERO 40mcg 120-Dose due to out of specification test results for impurities during stability testing. For Customer Service related questions – Contact TEVA CUSTOMER SERVICE at 1-800-545-8800. For Medical related questions – Contact MEDICAL INFORMATION at 1-888-838-2872 – OPTION 9. Affected product started shipping July 2, 2012 to present. Please check your inventory for the above product and lot number. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


February 11, 2014


Retail Level Recall



Product:TRUEbalance Blood Glucose Meters
Moore's Re-order#: 88480, 93605
Lot #:KK0468, KL01079, KM0337TI, KN1834TI, KN1973TI, , KN2089TI, KN2090TI,KN2102TI, KP0047TI, KP0076TI, KP0128TI, KP0925TI, KN2074TI

Manufacturer:NIPRO DIAGNOSTICS

PRODUCT SUBJECT TO RECALL

NIPRO is contacting customers on behalf of Moore Medical LLC. If you have any questions please cal: Stericycle @ 1-866-236-4518.

Please check your inventory for the above product and lot number. A letter from NIPRO describing the procedure will follow via mail to customers who purchased this product in the past.


February 11, 2014


Retail Level Recall



Product:TRUEtrack Blood Glucose Monitor
Moore's Re-order#: 84223, 84422
Lot #:KJ0731, KK0964, KL01213,KL01233-3TI, KL0267-10, KL0381-14,KL0637-2TI, KL0716TI, KL0860TI, KP0074TI

Manufacturer:NIPRO DIAGNOSTICS

PRODUCT SUBJECT TO RECALL

NIPRO is contacting customers on behalf of Moore Medical LLC. If you have any questions please cal: Stericycle @ 1-866-236-4518.

Please check your inventory for the above product and lot number. A letter FROM NIPRO describing the procedure will follow via mail to customers who purchased this product in the past.


February 11, 2014


Retail Level Recall



Product:Levothyroxine Tablets
Moore's Re-order#: 10616
Lot #:3037531, 3038284

NDC 0378-1819-01

Manufacturer:Mylan Pharma/McKesson

PRODUCT SUBJECT TO RECALL

Moore Medical LLC, received the following recall from Mylan Pharmaceuticals/McKesson Pharma. Mylan is conducting a voluntary recall of two lots, referenced below, of Levothyroxine Sodium Tablets 100’s, UPS. These lots are being recalled due to composite assay results obtained during routine stability testing that were slightly below the specification. These lots were distributed May 8, 2012 to present.

Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchase this product in the past.


January 17, 2014


Retail Level Recall



Product:GARDASIL®
Moore's Re-order#: 81791
Lot #:J007354

NDC 00006-4045-41

Manufacturer:Merck

PRODUCT SUBJECT TO RECALL

Merck is voluntarily recalling this product due to the potential for a limited number of vials to contain glass particles. Merck’s investigation concluded that for certain vials in the affected lot, the potential exists for small glass particles to be present in the vial. If a vaccine containing glass particles is administered to a patient, there is a remote risk of an injection site reaction. The sterility of the vaccine has not been impacted. Please call Sterycicle, Inc. at 1-855-741-4996 for product return instructions. Please do not return any product to Moore Medical.

This lot was distributed by Merck August 20, 2013 to present. Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


January 17, 2014


Retail Level Recall



Product:Menveo
Moore's Re-order#: 93988
Lot #:M12188

Manufacturer:GSK (GlaxoSmithKline)

PRODUCT SUBJECT TO RECALL

GSK(GlaxoSmithKline) is implementing a voluntary market recall of one lot of MENVEO- Meningococcal (Groups A-C-Y and W-135) Oligosaccharide Diphtheria CRM-197 Conjugate Vaccine. This precautionary and voluntary action is being taken following observation of higher-than-specified levels of residual moisture within the lyophilized MenA component vial in the lot noted. This residual moisture content is not expected to impact product quality but constitutes a deviation to registered specification. All other aspects of this lot have met the required quality standards. GSK/Novartis Vaccines is not aware of any safety issues that could arise due to higher moisture content.

IT IS IMPORTANT TO NOTE THAT NO ACTION IS REQUIRED FOR PATIENTS PREVIOUSLY VACCINATED WITH A DOSE FROM THIS LOT.

Affected product started shipping May 15, 2013 to present. Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


January 17, 2014


Retail Level Recall



Product:Scrub Care® Surgical Scrub Brushes
Moore's Re-order#: 72945
Lot #:All Lot Numbers – Product Code 4452B

Manufacturer:CareFusion

PRODUCT SUBJECT TO RECALL

CareFusion is conducting a voluntary recall/removal of CareFusion Scrub Care Surgical Scrub Brush-Sponge/Nail Cleaner, Product Code 4452B. The available iodine in the product is less than as stated on the product label & therefore does not meet the label claim for free iodine concentration. Although the efficacy of the product is expected to be reduced, the use of the scrub brush is one of several elements involved in preparation for patient care. CareFusion has received zero (0) complaints involving adverse patient/user impact. CareFusion is advising customers to DESTROY ALL PRODUCT. DO NOT RETURN the product to CareFusion. DO NOT contact CareFusion with any questions regarding credits, stock destruction or substitution products.

Affected product was distributed March 2013 to present. Please check your inventory for the above product and lot number. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


January 10, 2014


Retail Level Recall



Product:Folic Acid 5mg/mL Multi Dose Vial
Moore's Re-order#: 11727
Lot #:6104649, 6104789, 6105069

NDC 6332318411

Manufacturer:Fresenius Kabi

PRODUCT SUBJECT TO RECALL

Fresenius Kabi, USA, LLC (“Fresenius Kabi”) , formerly APP Pharmaceuticals, LLC, is voluntarily recalling Folic Acid Inj USP 5mg/ml 10ml MDV. Fresenius Kabi is taking this action due to an out-of-specification result reported for impurities at the 15 and 14 month stability test station for the first two lots referenced, respectively. The third lot remains within specification to date, however based on the root cause analysis, it is expected to exhibit the same behavior prior to expiry. The investigation reveals that this issue is limited to the three product lots listed. The Health Hazard Evaluation concluded that while the increased degradation of Folic Acid Injection, which leads to production of an inactive metabolite, could potentially decrease the concentration of the active molecule, Folic Acid concentration remained within the specific range. As a result, the hazard risk of product administration is assessed as low.

These lots started shipping September 30, 2012 to present.

Please check your inventory for the above product and lot number. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


December 23, 2013


Retail Level Recall



Product:FreeStyle Test Strips
Moore's Re-order#: 79739
Lot #:1285007

Manufacturer:Abbott Diabetes Care

PRODUCT SUBJECT TO RECALL

Recently Abbott Diabetes Care became aware that certain lots of FreeStyle and FreeStyle Lite Blood Glucose Test Strips produce erroneously low blood glucose results when using FreeStyle Blood Glucose Meters, FreeStyle Flash Blood Glucose Meters and the FreeStyle blood glucose meter built into the Omnipod System. Erroneously low results that are not recognized may pose significant risks to a user’s health.

If you have any affected product, please take the following steps:

1.Call Abbott Diabetes Care Customer Service immediately at 1-888-736-9869 for replacement of the affected test strips. When you call, Abbott will send you unaffected FreeStyle and FreeStyle Lite Blood Glucose Test Strips at no charge.
2. While waiting for your replacement strips to arrive, either use an alternate method to measure your blood glucose (such as test strips from an unaffected lot number or a different blood glucose monitoring system). This issue only affects the lot numbers which are detailed above when using FreeStyle Blood Glucose Meters, FreeStyle Flash Blood Glucose Meters.

This lot was distributed from November 28, 2012 to the present. Please check your inventory for the above product and lot number. A letter describing the procedure to return any affected product will follow via mail to customers who purchased this product in the past.

Please do not return this to Moore Medical.


December 23, 2013


Retail Level Recall



Product:Sodium Chloride Injection USP Excel Bag
Moore's Re-order#: 69414
Lot #:NDC 0264-7802-00

Manufacturer:B. Braun Medical Inc.

PRODUCT SUBJECT TO RECALL

B. Braun recently identified an error in the barcode for some units contained in the product lot listed above. Both the bag label, printed in blue and the bag contents are accurate (0.45% Sodium Chloride Injection USP, NDC# 0264-7802-00, Lot#J3D548). However, the machine readable(scannable) barcode, printed in white at the top of the bag, may incorrectly reference 0.15% Sod Chlor Inj 20mEqK+/liter (NDC#0110302647865002,Exp Date/Lot# 1715040010J3D549). B. Braun has not received any reports of adverse events related to this lot to date. Patients reporting any problems that may be related to the use of this product should be advised to contact a physician & report all issues to B Braun @ 800-854-6581.

Shipping of this product started May 2013 to present.

Please check your inventory for the above product and lot number. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


December 23, 2013


Retail Level Recall



Product:Freestyle Lite Test Strips
Moore's Re-order#: 94227
Lot #:1283345

Manufacturer:Abbott Diabetes Care

PRODUCT SUBJECT TO RECALL

Recently Abbott Diabetes Care became aware that certain lots of FreeStyle and FreeStyle Lite Blood Glucose Test Strips produce erroneously low blood glucose results when using FreeStyle Blood Glucose Meters, FreeStyle Flash Blood Glucose Meters and the FreeStyle blood glucose meter built into the Omnipod System. Erroneously low results that are not recognized may pose significant risks to a user’s health.

If you have any affected product, please take the following steps:

1.Call Abbott Diabetes Care Customer Service immediately at 1-888-736-9869 for replacement of the affected test strips. When you call, Abbott will send you unaffected FreeStyle and FreeStyle Lite Blood Glucose Test Strips at no charge.
2. While waiting for your replacement strips to arrive, either use an alternate method to measure your blood glucose (such as test strips from an unaffected lot number or a different blood glucose monitoring system). This issue only affects the lot numbers which are detailed above when using FreeStyle Blood Glucose Meters, FreeStyle Flash Blood Glucose Meters.

This lot was distributed from November 28, 2012 to the present.

Please check your inventory for the above product and lot number. A letter describing the procedure to return any affected product will follow via mail to customers who purchased this product in the past.

Please do not return this to Moore Medical.


December 3, 2012


Retail Level Recall



Product:Sodium Chloride Injection USP 0.9%
Moore's Re-order#: 67061
Lot #:P292326 & P293993

Manufacturer:Baxter Healthcare Corporation

PRODUCT SUBJECT TO RECALL

Baxter Healthcare Corp is issuing a voluntary recall for the IV solution, 0.9% Sodium Chloride 100mL, due to particulate matter found in the solution. The root cause for this issue has been identified and resolved. If infused, particulate matter could lead to pulmonary embolism or irritation of the vein. Particulate matter identified prior to infusion may result in a delay in initiation or interruption of therapy. There have been no adverse events reported for this issue. This lot was distributed between May 2012 to the present.

Please check your inventory for the above product and lot number. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


November 27, 20113


Retail Level Recall



Product:Albuterol Sulfate Inhalation Solution
Moore's Re-order#: 88283
Lot #:A3A33A, A3A33B, A3A34A, A3A35A, A3A36A, A3A37A, A3A38A, A3A40A, A3A41A, A3A42A

Manufacturer:Nephron

PRODUCT SUBJECT TO RECALL

Nephron Pharmaceuticals initiated a voluntary recall as a precautionary measure, due to results from their internal monitoring processes. Nephron is asking consumers to discontinue use and return any product they may have that is included in this recall. Nephron performs aseptic process simulation as part of their internal processes to assure product quality. All lots listed met and passed Nephron’s quality specifications at the time of manufacture. Nephron has received no reportable adverse drug events for any of the lots included in this recall.

Please call Nephron at 800-443-4313 for return instructions.

Affected product started shipping August 5, 2013 to present. . Please check your inventory for the above product and lot number. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


November 4, 2013


Retail Level Recall



Product:Ciproflox
Moore's Re-order#: 15219
Lot #:3034630

NDC 51079018220

Manufacturer:Mylan Institutional Inc.

PRODUCT SUBJECT TO RECALL

Mylan Institutional Inc. is voluntarily recalling the item/lot listed due to GMP (Good Manufacturing Practice) compliance issues identified at the Smruthi Organics manufacturing facility. Affected lots were distributed under the UDL Laboratories, Inc. label. Affected product started shipping December 30, 2011 to present.

Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


November 4, 2013


Retail level Recall



Product:Prolia® Injection
Moore's Re-order#: 12931
Lot #:1037592

Manufacturer:Amgen

PRODUCT SUBJECT TO RECALL

Amgen is voluntarily recalling the item/lot of Prolia (denosumab) after identifying the presence of particulate matter which includes cellulose in a small number of pre-filled syringes (PFS) during a routine quality examination. No adverse events attributed to the presence of particulate matter which includes cellulose have been reported at the time of the recall. Amgen has conducted a thorough evaluation of the health risk and determined that the potential for adverse events is very low based on the size and characteristics of the particulate matter which includes cellulose.

Affected product started shipping June 26, 2013 to present.

Please check your inventory for the above product and lot number. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


October 3, 2013


Retail Level Recall



Product:HemoCue Glucose 201 Microcuvettes Single Pack
Moore's Re-order#: 75622, 87732, 81229
Lot #:1207670 to 1304544, 1207670 to 1304544, 1207670 to 1304544

Manufacturer:HemoCue

PRODUCT SUBJECT TO RECALL

HemoCue has become aware of a production related problem that affects single pack pouches for the above mentioned microcuvettes. If a single pack pouch is damaged, the microcuvette can be exposed to moisture which in some cases may lead to low false readings. Patient risk could occur if medical intervention is based on false low readings. Microcuvettes from affected lots must not be used and will be replaced with new product. Information on how this will be handled will be provided by your local HemoCue representative.

The root cause of the problem has been identified and the problem has been corrected in the manufacturing process. Affected product was shipped from August 2012 to present.

Please check your inventory for the above product and lot number. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


October 3, 2013


Retail Level Recall



Product:Heparin Lock Flush Syringe
Moore's Re-order#: 83393
Lot #:13A0084N,13d0824N

Manufacturer:Covidien

PRODUCT SUBJECT TO RECALL

Covidien is voluntarily recalling specific lots of Monoject Prefill Flush Syringes. This recall is being conducted due to the risk that some syringes in these lots were not sterilized and in addition may contain water rather than saline or heparin as indicated on the label. Covidien is unaware of any adverse events associated with the listed product These items were produced during January 2013 to present.

Please check your inventory for the above product and lot number. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


October 3, 2013


Retail Level Recall



Product:Diazepam Injection USP
Moore's Re-order#: 84751
Lot #:23-505-EV* (Note: the lot # may be followed by 01)

NDC #0409-3213-12

Manufacturer:Hospira

PRODUCT SUBJECT TO RECALL

Hospira, Inc., is voluntarily recalling this lot of Diazepam Injection, USP, due to a customer report of leaking at the neck of the vial. This may result in a potential breach of sterility/contamination of the vial contents and/or leakage of contents. A loss of sterility is a primary concern when a container has a leak, since an open pathway exists for contamination of fluid. If contaminated solution is used on a patient, this may potentially cause bacteremia, sepsis, septic shock, endocarditis and death may result. Signs & symptoms could include redness, pain, swelling at the site, fever, shortness of breath, tachycardia, nausea and vomiting. Injections of contaminants may potentially lead to septicemia which may require critical medical intervention. Additionally, there is the potential for leakage of contents.

To date, Hospira has not received reports of any adverse events associated with this issue for this lot. Root cause has been identified and corrective & preventive actions have been initiated to address this event. This lot was distributed from March 2013 to present.

Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


October 3, 2013


Retail Level Recall



Product:Scotchcast™ Wet or Dry Cast Padding
Moore's Re-order#: 80995, 80996, 80997, 80998
Lot #:792920, 793090, 793640, 796078, 792921, 793098, 793638, 796077, 798487, 792922, 793116, 793637, 796079, 798488, 792923, 793636, 798489, 799235, 799236

Manufacturer:3M

PRODUCT SUBJECT TO RECALL

3M is conducting a voluntary recall of selected lots of 3M Scotchcast Wet or Dry Padding following a determination that the cast padding material does not consistently repel water. Lack of repellency may result in prolonged cast dry times after exposure to wet conditions. There have been no reports of patient injury associated with this material to date. 3M is voluntarily recalling the product to minimize the potential of skin maceration under a cast exhibiting inconsistent repellency characteristics. This field setting action involves material only with affected Catalog and Lot Numbers provided. 3M Scotchcast Wet or Dry currently, at the end user setting, may be USED UNDER DRY CONTITIONS ONLY until replacement product is available. Care must be taken to ensure that the change in directions for use is clearly communicated to health care providers and patients receiving casts.

These lots were shipped May 2013 to present. 3M SCOTCHCAST WET OR DRY CAST PADDING CATALOG NUMBER(S) ARE: WDP2, WDP3, WPD4, WDP6.

Please check your inventory for the above product and lot number. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


October 3, 2013


Retail Level Recall



Product:Ketorolac Tromethamine
Moore's Re-order#: 77081
Lot #:25-048DK* (Lot number may be followed by 01)

Manufacturer:Hospira

PRODUCT SUBJECT TO RECALL

Hospira, Inc. is voluntarily recalling the item/lot listed above due to customer report that either a loose crimp or no crimp was applied to the fliptop vial. Affected product started shipping February 2013 to present. Please check your inventory for the above product and lot number. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


October 3, 2013


Retail Level Recall



Product:Prednisone Tablets
Moore's Re-order#: 14351
Lot #:261739A

Manufacturer:Roxane Laboratories

PRODUCT SUBJECT TO RECALL

Roxane Laboratories, Inc is voluntarily initiating a recall due to two reports of missing labeling for the unit dose blister cards within this one lot. For medical or technical product information, call 800-962-8364 and select option 6. Affected product started shipping March 2013 to present. Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


October 3, 2013


Retail Level Recall



Product:Aminosyn 10% Solution
Moore's Re-order#: 96880
Lot #:26-138-JT (NOTE: the lot number may be followed by 01)

Manufacturer:Hospira

PRODUCT SUBJECT TO RECALL

Hospira, Inc. is voluntarily recalling one lot of Aminosyn II 10% due to a confirmed customer report of particulate. The particulate was confirmed as human hair, sealed between the port tube and the body of the bag at the mandrel seal of the primary container. The presence of particulate may result in a potential delay of therapy and/or a potential for a local inflammatory reaction if infused into the patient. If the particulate matter is not detected until the point of care, there may be a delay in therapy, which depends on the time required to obtain a replacement container & compound the admixture. If the particulate breaks & pieces are able to pass thru the intravenous catheter, injected particulate material may result in local inflammation, phlebitis and/or low-level allergic response. Capillaries, which may be as small as the size of a red blood cell, may become occluded. Patients with preexisting conditions of trauma or other medical conditions that adversely affects the microvascular blood supply are at an increased risk. To date, Hospira has not receiver reports of any adverse events associated with this issue for this lot.

This lot was distributed March 2013 to present.

Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


October 3, 2013


Retail Level Recall



Product:Theraflu PE Severe Cold Day
Moore's Re-order#: 91003
Lot #:10115840, 10115888, 10118946, 10118948, 10119864, 10119867, 10122271, 10122297, 10122300, 10124374, 10124493, 10125910, 10128097, 10128099, 10128101

Manufacturer:Novartis Consumer Health, Inc

PRODUCT SUBJECT TO RECALL

Novartis consumer Health, Inc. (NCH) is voluntarily recalling all lots and SKUs of over-the-counter cough/cold product Theraflu powders in the United States. The list of all lots was provided by Novartis. These lots are being recalled because they contained trace amounts of impurities, which they do not believe pose safety issues. Affected product started shipping July 2010 to present. Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


October 3, 2013


Retail Level Recall



Product:Metoclopramide Injection
Moore's Re-order#: 74651
Lot #:28-104-DK* *Lot number(s) may be followed by 01

NDC #00409341401

Manufacturer:Hospira

PRODUCT SUBJECT TO RECALL

Hospira, Inc., is voluntarily recalling the items/lots listed due to a confirmed vial defect where spiticule (glass strands) were identified as being affixed to the inside of the vial walls. There is a potential for the glass particulates to dislodge into the solution. Hospira has not received reports of any adverse events with this issue for these lots. Affected product started shipping June 2013 to present. Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


October 3, 2013


Retail Level Recall



Product:Ondansetron Injection USP
Moore's Re-order#: 86446
Lot #:29-484-DK*, 29-501-DK* *Lot number(s) may be followed by 01

NDC #00409475503

Manufacturer:Hospira

PRODUCT SUBJECT TO RECALL

Hospira, Inc., is voluntarily recalling the items/lots listed due to a confirmed vial defect where spiticule (glass strands) were identified as being affixed to the inside of the vial walls. There is a potential for the glass particulates to dislodge into the solution. Hospira has not received reports of any adverse events with this issue for these lots. Affected product started shipping June 2013 to present. Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


August 9, 2013


Retail Level Recall



Product:Gastrografin Solution
Moore's Re-order#: 14718
Lot #:00500512

NDC 0270-0445-40

Manufacturer:Bracco Diagnostics Inc

PRODUCT SUBJECT TO RECALL

Bracco Diagnostics Inc. is voluntarily recalling, from the market, one (1) lot of Gastrografin. This voluntary recall has been initiated due to a customer complaint received regarding foreign particles in this lot of Gastrografin. At this time, there are no other lots of Gastrografin affected by this action. Bracco Diagnostics Inc. is contacting customers directly and no products will be return to Moore Medical LLC.

Affected products started shipping March 2013 to present. Please check your inventory for the above product and lot number. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


August 9, 2013


Retail Level Recall



Product:Sodium Chloride 0.9% 250mL
Moore's Re-order#: 54304
Lot #:16-031-JT (Lot numbers may be followed by 01 or 02)

NDC 0409-7983-02

Manufacturer:Hospira, Inc.

PRODUCT SUBJECT TO RECALL

Hospira Inc., is voluntarily recalling one lot of 0.9% Sodium Chloride Injection USP due to the potential for solution to leak at or near the administrative port of the primary container. This may result in a potential breach of sterility, contamination of the primary container contents and leakage of contents. When a primary container within an overwrap has a leak, there is an open pathway for contamination of the product.

Patients intravenously injected with this product may have the potential to be at risk for septicemia. The use of contaminated solution could result in significant patient harm requiring immediate medical attention. Signs and symptoms may include injection site reactions, fever, shortness of breath, fast heart rate and feeling generally ill with nausea and vomiting.

Additionally, leakage of solution from the primary container may potentially result in drug wastage & spillage onto equipment, flooring and personnel. Leakage from the primary container may result in a potential for inadequate or inconsistent solution/medication dosing and/or a delay in therapy.

This lot was distributed July 2012 to present. Please check your inventory for the above product and lot number. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


August 9, 2013


Level Recall



Product:Oxytocin Injectable Emulsion SDV
Moore's Re-order#: 74653
Lot #:6003648

NDC 63323-012-0

Manufacturer:Fresenius Kabi USA, LLC

PRODUCT SUBJECT TO RECALL

Fresenius Kabi USA, LLC is voluntarily recalling this product lot. Fresenius Kabi USA, LLC has decided to take this action due to an out-of-specification result for assay at the 15-month stability test station. The preliminary investigation reveals that this issue is limited to the one product lot indicated. As a precautionary measure, Fresenius Kabi is recalling Oxytocin Injection, UPS (Synthetic) 10 USP units/ml. Patient response to exogenously administered oxytocin is characterized by significant inter-and intra-patient variability. Administration of this drug should be closely monitored and the dose should be adjusted based on the patient response. No adverse events have been received for Oxytocin Injection, USP (Synthetic). Due to the variability of the clinical effect of oxytocin, the risk to patient safety is considered to be moderate.

Affected product was shipped May 2012 to present. Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchase this product in the past.


August 9, 2013


Retail Level Recall



Product:Cefazol Injection
Moore's Re-order#: 87864
Lot #:DB2208

NDC 00781345196

Manufacturer:Sandoz

PRODUCT SUBJECT TO RECALL

Sandoz is voluntarily recalling the above item/lot due to a customer complaint received for broken vials associated with this lot of product. Product started shipping March 2013 to present. Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


August 9, 2013


Retail Level Recall



Product:Propofol
Moore's Re-order#: 88089
Lot #:10-101-DJ, 10-102-DJ. NOTE: the lot number may be followed by 01

Manufacturer:HOSPIRA

PRODUCT SUBJECT TO RECALL

Hospira, Inc. is voluntarily recalling these lots of Propofol Injectable Emulsion due to a single visible particulate identified during a retain sample inspection. The presence of visible particulate in Propofol may potentially cause a delay in therapy and if administered has the potential for patient injury where small capillaries may become occluded. Injected particulate matter may potentially result in local inflammation, phlebitis and /or low level allergic response through mechanical disruption of tissue or immune response to the particulate. Small capillaries may become occluded. Chronically, following sequestration, granulomatous formation in the lungs is possible.

Distribution of these lots started February 2012 to present. Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


August 9, 2013


Retail Level Recall



Product:CIDEX OPA Solution
Moore's Re-order#: 64477
Lot #:20390

Manufacturer:ASP/Johnson & Johnson

PRODUCT SUBJECT TO RECALL

Advanced Sterilization Products/Johnson & Johnson has discovered instances of missing labels on bottles of CIDEX OPA Solution. Four complaints have been received from customers and ASP has determined that from their records you may have received bottles of CIDEX OPA Solution with missing labels. ASP is asking customers to take inventory of their CIDEX OPA Solution supply and check each bottle for a label.

This lot was manufactured from May 2011 to present. Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


August 9, 2013


Retail level Recall



Product:Ondansetron
Moore's Re-order#: 86446
Lot #:25-394-DK

NDC 00409475503

Manufacturer:Hospira

PRODUCT SUBJECT TO RECALL

Hospira, Inc., is voluntarily recalling this item/lot due to the solution potentially having come in contact with polyethylene particulate while being processed. Affected products started shipping February 2013 to present. Please check your inventory for the above product and lot number. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


August 9, 2013


Retail Level Recall



Product:Cleocin Phosphate
Moore's Re-order#: 14329
Lot #:G34910 6/14, G36879 7/14, G41005 7/14, G53478 9/14, G63444 10/14, G76317 11/14

Manufacturer:Pfizer

PRODUCT SUBJECT TO RECALL

Pfizer, Inc. is recalling the above referenced lots of Cleocin Phosphate (ADD-Vantage Vial). Pfizer, Inc. voluntarily initiated this recall when it was determined that these lots may contain a small number of vials with very small reflective flakes consistent with delamination of the glass vial.

Affected product started shipping August 2012 to present. Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


August 9, 2013


Retail Level Recall



Product:Cleocin Phosphate
Moore's Re-order#: 14329
Lot #:G34910 6/14, G36879 7/14, G41005 7/14, G53478 9/14, G63444 10/14, G76317 11/14

Manufacturer:Pfizer

PRODUCT SUBJECT TO RECALL

Pfizer, Inc. is recalling the above referenced lots of Cleocin Phosphate (ADD-Vantage Vial). Pfizer, Inc. voluntarily initiated this recall when it was determined that these lots may contain a small number of vials with very small reflective flakes consistent with delamination of the glass vial.

Affected product started shipping August 2012 to present. Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


January 25, 2013


Retail Level Recall



Product:Hyfrecator Electrodes
Moore's Re-order#: 34639, 44519
Lot #:Beginning Lot 120628x Ending Lot 120917X and Beginning Lot 120628X Ending Lot 120917X

Manufacturer:ConMed

PRODUCT SUBJECT TO RECALL

ConMed has issued this recall due to a packaging issue with certain ConMed Electrosurgery Disposable Active Electrodes and Accessories. ConMed received complaints of some devices which had broken through the seal of the sterile pouch. ConMed has confirmed instances where the pouch seal was compromised on the affected products. In no instance has it been reported to ConMed Corp that a compromise in the sterile barrier has resulted in illness or injury.

ConMed Corp has decided to recall the devices, therefore, please stop use of these devices immediately. Please do not return used devices. These items were shipped beginning 6/28/12 to present.


January 25, 2013


Retail Level Recall



Product:Electrosurgical Tip Cleaner
Moore's Re-order#: 83889
Lot #:Beginning Lot 120628X Ending Lot 120725X

Manufacturer:ConMed

PRODUCT SUBJECT TO RECALL

ConMed has issued this recall due to a packaging issue with certain ConMed Electrosurgery Disposable Active Electrodes and Accessories. ConMed received complaints of some devices which had broken through the seal of the sterile pouch. ConMed has confirmed instances where the pouch seal was compromised on the affected products. In no instance has it been reported to ConMed Corp that a compromise in the sterile barrier has resulted in illness or injury.

ConMed Corp has decided to recall the devices, therefore, please stop use of these devices immediately. Please do not return used devices. These items were shipped beginning 6/28/12 to present.


January 11, 2013


Retail Level Recall



Product:Nalbuphine HCl Fliptop Multiple Dose Vial
Moore's Re-order#: 58158
Lot #:11-293-DK, NDC# 0409-1467-01

Manufacturer: Hospira

PRODUCT SUBJECT TO RECALL

Hospira,Inc is voluntary recalling one lot of Nalbuphine HCI Injection to the user level, due to two confirmed customer reports: one report of a loose crimp applied to the fliptop vial and one report of a missing vial stopper and fliptop cap. This may result in an open system and potential for contamination and compromised sterility. If contaminated solution is used on a patient, critical patient harm may result and may potentially lead to septicemia which in worst case scenario may have the potential to progress to septic shock which may be life threatening. Signs and symptoms could include injection site reactions, fever, shortness of breath, fast heart rate and feeling generally ill with nausea and vomiting. These lots were distributed July 2012 through present.

Please check your inventory for the above product and lot number. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


january 11, 2013


Retail Level Recall



Product:BD Vacutainer® Citrate Tubes Plastic Buffered Sodium Citrate 0.109M / 3.2%
Moore's Re-order#: 67843
Lot #:2180434

Manufacturer:BD

PRODUCT SUBJECT TO RECALL

BD is conducting a recall of the BD Vacutainer 2.7ml Plus Citrate Blood Collection Tube due to extended Partial Thromboplastin Time (aPTT) test results. BD’s internal investigation indicates that aPTT measured using the affected tubes may be falsely elevated. Erroneous aPTT may result in inappropriate decisions regarding patient care. These lots were distributed August 1, 2012 through present.

Please check your inventory for the above product and lot number. A letter will follow via mail from BD to customers who purchased this product in the past.


November 20, 2012


Retail Level Recall



Product:Epinephrine
Moore's Re-order#: 86974, 52909
Lot #:100953A, 120803A, 100953A, 120803A

NDC# 0409-7241-01 and 0409-7241-01

Manufacturer:Hospira

PRODUCT SUBJECT TO RECALL

Hospira is voluntarily recalling two lots of Epinephrine Injection, USP identified above due to one confirmed customer report of an Epinephrine ampule containing visible particulate. Upon examination of retained samples of the potentially impacted lots, Hospira found several ampules which contained small glass particles. In the event a healthcare professional injects glass particulate matter into a patient there may be the potential for critical patient injury. If administered intravenously, the risks associated with this defect may have the potential to result acutely in local inflammation, phlebitis, and/or generalized low-level allergic response and/or embolize to other organs in the body. Hospira has received no reports of adverse events associated with these product lots.

This product was shipped January 2012 to present. Please check your inventory for the above product and lot numbers.


October 30, 2012


Retail Level Recall



Product:Cholestech LDX Multiananlyte Control
Moore's Re-order#: 96356
Lot #:C2510 & C2510A

Manufacturer:Alere

PRODUCT SUBJECT TO RECALL

In response to complaints, Alere has investigated the above listed lot numbers and confirmed these lots may yield results which are out of range high for the Level 2 control when tested with Alere Cholestech LDX HDL test. You should wait until you receive the letter from Alere with instructions to discard it and how to receive replacement product. Customers will not be returning the product to Moore Medical.

This product was shipped July 2012 to present. Please check your inventory for the above product and lot numbers.


October 15, 2012


Retail Level Recall



Product:ProTime3 Cuvettes PRO3-25
Moore's Re-order#: 76587
Lot #:Cuvette Pouch Lot # B2P3C033, B2P3C039, C2P3C049, C2P3C055, M1P3C480

Kit Lot # B2K3C033, B2K3C039, C2K3C049, C2K3C055, M1K3C480

Manufacturer:ITC (International Technidyne Corp)

PRODUCT SUBJECT TO RECALL

Moore Medical LLC has received a recall notice from ITC, involving the ProTime3 Cuvettes . The purpose of this letter is to provide important information regarding certain lots of ProTime3 Cuvettes. An essential part of ITC’s quality system is continuous product performance surveillance. During this surveillance ITC has determined that some ProTime3 Test Cuvettes (PRO3-25) within the specified lot range may recover lower than expected Prothrombin Time/International Normalized Ratio (PT/INR) results. The company’s investigation into the product’s performance identified increased imprecision in addition to an increased negative bias, the combination of which may manifest as lower than expected PT/INR test results.

ITC is implementing corrective actions to restore product performance. This recall does not involve the ProTime instrument. Distribution records indicate that at least one box of an affected lot of ProTime3 Cuvettes was shipped to your facility. This product was shipped April 2012 to present.

Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


October 10, 2012


Retail Level Recall



Product:Typhim Vi Typhoid Vial
Moore's Re-order#: 86734
Lot #:G1130-1

NDC# 49281-790-20

Manufacturer:Sanofi Pasteur

PRODUCT SUBJECT TO RECALL

Sanofi Pasteur is voluntarily recalling some lots of Typhim Vi vaccine (prefilled syringes and 20-dose vials). The vaccine met all release requirements at the time of distribution. Sanofi Pasteur is taking this action because these lots are at risk for lower antigen content. There is no safety concern related to this action. These products were shipped January 2011 to present.

Please check your inventory for the above products and lot numbers. A letter describing the procedure to return any affected products to Moore Medical will follow via mail to customers who purchased these products in the past.


October 11, 2012


Retail Level Recall



Product:0.9% Sodium Chloride Injection, 1000 mL
Moore's Re-order#: 10214
Lot #:08-163-JT, 90-036-JT, 02-048-JT

NDC# 0409-7983-48

Manufacturer:Hospira

PRODUCT SUBJECT TO RECALL

This recall has been initiated due to the potential for solution to leak. This can result in an open system which has the potential for contamination, compromised sterility, drug wastage and/or spillage, inadequate or inconsistent dosing, and delay in therapy, all of which may require medical intervention and should be reported to Hospira. Hazardous exposure is a potential risk for the patient and/or healthcare provider in the event a hazardous drug is added to the flexible container. Regardless, if used on a patient or in an inpatient care setting, these compromised solutions have the potential to result in injury requiring medical intervention for the patient and/or healthcare provider. This product was shipped June 2011 to present.

Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


October 11, 2012


Retail Level Recall



Product:0.9% Sodium Chloride Injection, 250mL
Moore's Re-order#: 54304
Lot #:93-102-JT

NDC# 0409-7983-02

Manufacturer: Hospira

PRODUCT SUBJECT TO RECALL

This recall has been initiated due to the potential for solution to leak. This can result in an open system which has the potential for contamination, compromised sterility, drug wastage and/or spillage, inadequate or inconsistent dosing, and delay in therapy, all of which may require medical intervention and should be reported to Hospira. Hazardous exposure is a potential risk for the patient and/or healthcare provider in the event a hazardous drug is added to the flexible container. Regardless, if used on a patient or in an inpatient care setting, these compromised solutions have the potential to result in injury requiring medical intervention for the patient and/or healthcare provider. This product was shipped June 2011 to present.

Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


October 11, 2012


Retail Level Recall



Product:5% Dextrose Injection, 250mL
Moore's Re-order#: 54301
Lot #:Lot# 01-201-JT

NDC# 0409-7922-02

Manufacturer:Hospira

PRODUCT SUBJECT TO RECALL

This recall has been initiated due to the potential for solution to leak. This can result in an open system which has the potential for contamination, compromised sterility, drug wastage and/or spillage, inadequate or inconsistent dosing, and delay in therapy, all of which may require medical intervention and should be reported to Hospira. Hazardous exposure is a potential risk for the patient and/or healthcare provider in the event a hazardous drug is added to the flexible container. Regardless, if used on a patient or in an inpatient care setting, these compromised solutions have the potential to result in injury requiring medical intervention for the patient and/or healthcare provider. This product was shipped June 2011 to present

Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


October 11, 2012


Retail Level Recall



Product:Typhim Vi Typhoid Prefilled Syringe
Moore's Re-order#: 50889
Lot #:E1287-1, E1288-1, G0481-1, G0507-1, G0508-1

NDC# 49281-790-51

Manufacturer:Sanofi Pasteur

PRODUCT SUBJECT TO RECALL

Sanofi Pasteur is voluntarily recalling some lots of Typhim Vi vaccine (prefilled syringes and 20-dose vials). The vaccine met all release requirements at the time of distribution. Sanofi Pasteur is taking this action because these lots are at risk for lower antigen content. There is no safety concern related to this action. These products were shipped January 2011 to present.

Please check your inventory for the above products and lot numbers. A letter describing the procedure to return any affected products to Moore Medical will follow via mail to customers who purchased these products in the past.


September 27, 2012


Retail Level (Notice of Destruction) Recall



Product:Triad Alcohol Prep Pads ONLY in Kit
Moore's Re-order#: Triad Alcohol Prep Pads ONLY in Kit 88743
Lot #:Triad Alcohol Prep Pads ONLY – All Lots

Manufacturer:Wolf Medical / Triad Group

PRODUCT SUBJECT TO RECALL

Triad Group issued a voluntary recall of ALL LOTS of Alcohol Prep Pads due to potential microbial contamination. Please destroy TRIAD ALCOHOL PREP PADS ONLY. The use of contaminated Alcohol Prep Pads could lead to life-threatening infections, especially in at risk populations, including immune suppressed and surgical patients. The rest of the kit is fine.

This product was shipped January 2010 to present.

Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


September 27, 2012


Retail Level Recall



Product:InviroSnap Safety Syringe
Moore's Re-order#: 83543 , 83538, 83539 , 83541
Lot #:Lot: 2006-09, Lot: 2006-06, Lot: 2006-06, Lot: 2006-07

Manufacturer:Inviro Medical

PRODUCT SUBJECT TO RECALL

A complaint was received by Inviro Medical stating that when the plunger is retracted after an injection, the plunger with needle can be pulled out of the back of the syringe. During the investigation a manufacturing deviation was identified and corrected.

This product was shipped January 2006 to present.

Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


September 27, 2012


Retail Level Recall



Product:R2 Pediatric Non-Radiolucent Multifunction Electrodes
Moore's Re-order#: 73832
Lot #:1109234

Manufacturer:ConMed Corporation

PRODUCT SUBJECT TO RECALL

ConMed has received a complaint of four individual devices, which were assembled with an adult-sized electrode pad to the pediatric lead wire set and were packaged in the white color-coded adult pouch. Other than being packaged in the wrong pouches and being assembled to the wrong size electrode pads, ConMed Corp has no reason to suspect any issue with the product. Though the larger electrode pads will still provide the desired clinical effect without adverse health consequences and do not pose a risk to health. ConMed Corp has decided to remove the devices to the user level. Therefore, please stop the use of these devices immediately.

This product was shipped September 23rd, 2011 to present.

Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


September 27, 2012


Retail Level Recall



Product:Triad Povidone Iodine Products ONLY in kit 82764
Moore's Re-order#: Triad Povidone Iodine Products ONLY in kit 82764
Lot #:Triad Povidone Iodine Products ONLY 82764 82764MMC Moore Brand Incision/Drainage Pack Anything prior to 10IA (see ** below for explanation) **The first two numbers are the year and the third character is the month. So Lot# 10IA is September (I) 2010. A=January, B=February, C=March, D=April, E=May, F=June, G=July, H=August, I=September, J=October, K=November, L=December. Anything before September 2010 would be affected or expired. Anything after September 2010 would be okay to use.

Manufacturer:Medline Industries / H&P Industries (Triad Group)

PRODUCT SUBJECT TO RECALL

H&P Industries, Inc. (Triad Group) is voluntarily recalling all Povidone Iodine Products. This recall was initiated because products were manufactured without having in place a system for microbial testing at the time of release, without having a system for testing of incoming components, and without having procedures designed and established to prevent objectionable organisms in these drug products. The use of the products manufactured under these conditions presents a risk of infection in patients undergoing medical and surgical procedures. This recall is for Triad Povidone Iodine Products ONLY. The rest of the kit is fine.

This product was shipped January 2008 to present.

Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


September 14, 2012


Retail Level Recall



Product:Propoxyphene Napsylate & Acetaminophen Tablets 100mg/650mg
Moore's Re-order#: 78158
Lot #:All Lots

NDC# 0093-0890-05

Manufacturer:TEVA Pharmaceuticals

PRODUCT SUBJECT TO RECALL

TEVA Pharmaceuticals is withdrawing the following product. This product was shipped January 2005 to present.

Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


September 14, 2012


Retail Level (Notice of Destruction) Recall



Product:Triad Povidone Iodine Prep Pads ONLY in Kits
Moore's Re-order#: 90233, 90558, 92183, 93124
Lot #:All Lots

Manufacturer:Moore Medical / H&P Industries (Triad)

PRODUCT SUBJECT TO RECALL

H&P Industries, Inc.(Triad) is voluntarily recalling all Triad Povidone Iodine Products ONLY. The Triad Povidone Iodine Products should be destroyed. The rest of the kit is fine. This recall was initiated because products were manufactured without having in place a system for microbial testing at the time of release, without having a system for testing incoming components, and without having procedures designed and established to prevent objectionable microorganisms in these drugs. The use of these products manufactured under these conditions presents a risk of infection in patients undergoing medical and surgical procedures. These product were shipped 2009 to present.

Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


September 14, 2012


Retail Level (Notice of Destruction) Recall



Product:Triad Alcohol Pads, Swabs & Swab Sticks Only
Moore's Re-order#: 57819
Lot #:Triad Products ONLY, All Lots

Manufacturer:Pac-Kit

PRODUCT SUBJECT TO RECALL

Pac-Kit has received a voluntary product recall notice from Triad Group. Destroy ALL LOTS of Triad Group Alcohol Prep Pads, Swabs and Swab sticks manufactured by Triad Group. This product was shipped April 2010 to present.

Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


September 14, 2012


Retail Level (Notice of Destruction) Recall



Product:Triad PVP Iodine Wipes
Moore's Re-order#: 90401
Lot #:Triad PVP Iodine Wipes ONLY – All Lots

Manufacturer:Certified Safety

PRODUCT SUBJECT TO RECALL

One of Certified Safety’s vendors, H&P Industries, has issued a voluntary recall which includes ALL LOTS of Triad PVP Iodine Wipes. Destroy the Triad PVP Iodine Wipes ONLY. This product was shipped January 2010 to present.

Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


September 12, 2010


Retail Level (Notice of Destruction) Recall



Product:Triad Alcohol Pads
Moore's Re-order#: 92026
Lot #:All Lots

Manufacturer:Heritage Labs

PRODUCT SUBJECT TO RECALL

Recall of the TRIAD ALCOHOL PAD ONLY was initiated due to a possible contamination of the bacteria Bacillus cereus. The rest of the kit is fine to use. The recall notice from Heritage Labs International requests customers and end-users to stop using, or destroy the recalled Triad Alcohol Pads. Please destroy TRIAD ALCOHOL PADS ONLY. This product was shipped January 2010 to present.

Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


September 12, 2012


Retail Level (Notice of Destruction) Recall



Product:Triad Povidone Iodine Prep Pads
Moore's Re-order#: 94237, 95313, 97384
Lot #:94237 21096 21420 21421 21422 21423 21424 21910 21911 21912 21913 22151 22152 22289 22290 22344 22345 22346 22347 22725 22726 22727 22728 22946 22947 22948 22949

Same lots as 94237

97384 80-0072 ENDING IN 092909 092710 090810 090109 083109 082310 081109 081009 080709 050710 050409 042110 041510 041410 031710 012910 012810 012010 110810 101210 100410

Manufacturer:North American Rescue (NAR)

PRODUCT SUBJECT TO RECALL

North American Rescue has been notified that the Triad Group has initiated a re call for their Povidone Iodine Pads due to a potential contamination. Please destroy the TRIAD PROVIDONE IODINE PADS ONLY. T he rest of the kit is fine. Destroy the TRIAD POVIDONE IODINE PADS ONLY. This product was shipped April 2009 to present.

Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


September 10, 2012


Retail Level Recall



Product:Adult R2 Non-Radiolucent Multifunction Electrodes
Moore's Re-order#: 73833
Lot #:1010194

Manufacturer:ConMed Corporation

PRODUCT SUBJECT TO RECALL

During a product inspection for a separate issue, ConMed discovered three individual devices of Cat. No. 3200-1715, Lot 1010194, which were assembled without the white oval shield which covers the wire set's rivet connection to the electrode pad. If the white rivet cover is missing, the metal rivet is exposed. If the user removes the clear protective pad liner and does not notice that the rivet cover is missing (and the metal rivet is exposed) and subsequently applies the electrode pad to a patient, this may result in possible injury to the patient. This product was shipped October 2010 to present.

Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


September 10, 2012


Retail Level Recall



Product:Coumadin 5mg
Moore's Re-order#: 00903
Lot #:9H49374A

Manufacturer:Bristol-Myers Squibb Company

PRODUCT SUBJECT TO RECALL

Bristol-Myers Squibb has initiated a voluntary recall of one manufactured lot of Coumadin 5 mg tablets. This recall is a precautionary measure based on the Company's testing of tablets from a returned bottle in which a single tablet was found to be higher in potency than expected. If there is too much active ingredient, there may be an increased risk of bleeding. If there is a decrease of active ingredient, there may be an increase in the risk of clots which could lead to heart attack or stroke. A global safety assessment was conducted to evaluate a potential lack of efficacy and no unexpected patterns were identified. This product was shipped September 2009 to present.

Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


September 10, 2012


Retail Level Recall



Product:Zolpidem Tablets 10mg
Moore's Re-order#: 88208
Lot #:ZPSB11054-A

NDC #16714062201

Manufacturer:Northstar

PRODUCT SUBJECT TO RECALL

Northstar is voluntarily recalling this lot because of a single complaint of product contamination with foreign tablets. This product was shipped Auguest 2011 to present.

Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


September 5, 2012


Retail Level Recall



Product:EID Esophageal Intubation Detector
Moore's Re-order#: 74057
Lot #:90923A, 91222A, 00327A, 00518A, 00623A, 00831B, 01013A, 01103A, 01214A, 10110A, 10301B, 10423A, 10530A, 10602A, 10703A, 10804A, 11004A, 120104, 120414

Manufacturer:LMA

PRODUCT SUBJECT TO RECALL

LMA North America Inc. (LMA) has issued a voluntary recall of the Esophageal Intubation Detector (EID100) manufactured by Wolfe Tory Medical and LMA North America. The product is being recalled because LMANA has received a complaint that the Esophageal Intubation Detector Syringe has a potential to create a false positive if used on a patient during confirmation of intubation. This product was shipped January 2009 to present.

Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


September 5, 2012


Retail Level Recall



Product:Pepto Bismol Regular and Extra Strength
Moore's Re-order#: 92543 & 04549
Lot #:2018171953 & 2017171953

NDC# 37000001903 & 37000003204

Manufacturer:P&G

PRODUCT SUBJECT TO RECALL

P&G is voluntarily recalling these products because water used to rinse a product contact surface did not meet the specifications for our purified water system. This product was shipped January 2012 to present.

Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


September 5, 2012


Retail Level Recall



Product:Female Catheter
Moore's Re-order#: 74885
Lot #:Lot# 082827-1, 120007, 122274, 122275, 123171, 124446, 129582, 130627, 142572, 310433, 318007, 322167, 335514, 338383, 340211, 342044, 350053, 350054, 350055, 359272, 359989, 405523

Manufacturer:Teleflex Medical

PRODUCT SUBJECT TO RECALL

Teleflex Medical is issuing a voluntary recall because packaging may be compromised, and therefore the sterility of the product cannot be guaranteed. If non-sterile products are used, there is a possible risk of infection. This product was shipped November 2007 to present.

Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


August 31, 2012


Retail Level Recall



Product:MONOJECT™ Insulin Safety Syringe
Moore's Re-order#: 74098
Lot #:015806 through 033106

Manufacturer:Covidien

PRODUCT SUBJECT TO RECALL

Covidien is conducting a voluntary recall regarding specific lots of Monoject Insulin Safety Syringe with a volume of 3/10 and 1/2 mL. This recall is being conducted due to a molding issue that can allow the safety shield to separate from the syringe, exposing the needle, which could potentially result in a needle stick. Product ID and lot numbers are clearly visible on the unit package and shipping case labels. This product was shipped May 2010 to present.

Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


August 31, 2012


Retail Level Recall



Product:VENTOLIN® HFA Inhalation Aerosol
Moore's Re-order#: 86768
Lot #:1ZP7355

NDC# 0173-0682-20

Manufacturer:GlaxoSmithKline

PRODUCT SUBJECT TO RECALL

GlaxoSmithKline is recalling the Ventolin HFA Inhalers due to a potential for the content of albuterol per dose to be below specification. This product was shipped September 12th 2011 to present.

Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


08/28/2012


Retail Recall



Product:0.9% Sodium Chloride Injection USP, 250mL
Moore's Re-order#: 54304
Lot #:Lot# 11-063-JT, NDC# 0409-7983-02

Manufacturer:Hospira

PRODUCT SUBJECT TO RECALL

This recall has been initiated due to the potential for solution to leak. This can result in an open system which has the potential for contamination, compromised sterility, drug wastage and/or spillage, inadequate ate or inconsistent solution/medication dosing, and delay in therapy, all of which may require medical intervention and should be reported to Hospira. Hazardous exposure is a potential risk for the patient and/or healthcare provider in the event a hazardous drug is added to the flexible container. Regardless, if used on a patient or in an inpatient care setting, these compromised solutions have the potential to result in injury requiring medical intervention for the patient and/or healthcare provider. This product was shipped June 2011 to present.

Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.


08/28/2012


Retail Level (Notice of Destruction) Recall



Product:LDL Cholesterol Test Strips
Moore's Re-order#: 91263
Lot #:L201

Manufacturer:Cardio Chek

PRODUCT SUBJECT TO RECALL

This recall has been initiated due to concerns that during product surveillance PTS has recently discovered that the identified lot (L201) of LDL Cholesterol test strips is showing an over-recovery when tested against a reference method. Based on the available data and the observed low frequency of over-recovery, PTS has determined that t he degree of over-recovery does not present a health risk. Thus, this warrants that PTS take action to remove this product from the field and initiate a voluntary product recall.

Customers with any of this product in their possession must immediately discontinue use and dispose of their remaining inventory of L201. PTS will provide appropriate replacement for any product that is properly identified on the enclosed "Customer Acknowledgement and Confirmation." This product was manufactured 01/12/2012. If you have any questions, please contact PTS Customer Service toll-free at 877 -870-5610 or 1-317-870-5610 (outside the US).

Please check your inventory for the above product and lot number. A letter describing the procedure to destroy any affected product and to obtain replacements from the manufacturer will follow via mail to customers who purchased this product in the past.


05/31/2012


Retail Level (Notice of Destruction) Recall



Product:Nitrostat®
Moore's Re-order#: 64756
Lot #:V100670 (for 0.4mg) and V100546 (for 0.6mg)

NDC 0071041813

Manufacturer:Pfizer

PRODUCT SUBJECT TO RECALL

Pfizer Inc is recalling lot numbers listed below of Nitrostat 0.4mg and 0.6mg tablets. Pfizer Inc voluntarily initiated this recall when it was determined that there is a remote possibility that bottles of NITROSTAT 0.6MG LOT V100546 may be contained in four pack cartons of NITROSTAT 0.4MG LOT V100670. The Nitrostat 0.6mg lot V100546 is not intended for sale in the US market.

Please note that administration of the above mentioned lots of NITROSTAT 0.6MG LOT V100546 packaged in cartons of Nitrostat 0.4mg lot V100670 may cause temporary or medically reversible adverse health consequences and the probability of serious adverse health consequences is remote. This product was shipped March 2011 to present.

Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected product to Moore Medical will follow via mail to customers who purchased this product in the past.



March 1, 2012


Retail Level Recall



Product: CaviCide® Surface Disinfectant
Moore's Re-order#: 69182, 76158
Lot #:10-1301, 10-2301, 10-2302, 10-2328, 10-2328A, 10-2328B, 10-2331, 10-2333, 10-1334, 10-2334, 10-1335, 10-2335, 10-1342A, 10-1343, 10-2345, 10-1301, 10-2301, 10-2302, 10-2328, 10-2328A, 10-2328B, 10-2331, 10-2333, 10-1334, 10-2334, 10-1335, 10-2335, 10-1342A, 10-1343, 10-2345

Manufacturer:Metrex

PRODUCT SUBJECT TO RECALL

Mextrex Research would like to inform you of a voluntary recall that it is conducting on CaviCide more specifically, 15 lots of product containing the Spring Fresh Fragrance only. It has come to Metrex's attention that the affected lots of product containing this fragrance have caused an increase in reported health reactions in some individuals such as headache, nausea, and respiratory discomfort.

CaviCide containing the Spring Fresh Fragrance meets all acceptable specifications for efficacy. Metrex is conducting this voluntary recall to ensure that none of its customers could potentially be exposed to a situation where they may experience any health discomfort. These products were shipped starting December 2010 to present.

Please check your inventory for the above products and lot numbers. A letter describing the procedure to return any affected products will follow via mail to customers who purchased this product in the past.


February 24, 2012


Retail Level Recall



Product:Dextrose 5% in Water (D5W)
Moore's Re-order#: 54301
Lot #:Lot# 95-067-JT (Lot number may be followed by 01) NDC# 0409-7922-02

Manufacturer:Hospira

PRODUCT SUBJECT TO RECALL

Hospira, Inc. is voluntarily recalling one lot of 5% Dextrose Injection, USP because there is a potential for solution to leak from a tear near the perimeter seal and the hanger slot. This can result in inadequate or inconsistent solution / medication dosing, delay in therapy, drug wastage, and / or spillage. In the unlikely event that the fluid seeps back into the bag, the fluid in the bag could become contaminated.

Hospira has initiated an investigation to determine the cause and preventative actions. Hospira has not received reports of any adverse events associated with this issue. This recall is being conducted as a precautionary measure. This lot was shipped December 2010 to present.

Please check your inventory for the above product and lot number. A letter describing the procedure to return any affected product will follow via mail to customers who purchased this product in the past.


February 24, 2012


Retail Level Recall



Product:Sodium Chloride 0.9% (NACL) 500mL
Moore's Re-order#: 54305
Lot #:06-830-FW (Lot number may be followed by 01, 02, or 03) NDC# 0409-7983-03

Manufacturer:Hospira

PRODUCT SUBJECT TO RECALL

Hospira, Inc. is voluntarily recalling one lot of 0.9% Sodium Chloride Injection, USP due to confirmed out of specification result for pH during lot specific protocol pH testing.

Please check your inventory for the above products and lot numbers. A letter describing the procedure to return any affected products will follow via mail to customers who purchased these products in the past.


Retail Level (Notice of Destruction) Recall


February 13, 2012



Product:Skin Prep Tray
Moore's Re-order#: 65740
Lot #:Various

Manufacturer:CareFusion

PRODUCT SUBJECT TO RECALL

The purpose of this letter is to notify you of a voluntary field removal (recall) initiated by CareFusion regarding CareFusion Skin Prep Tray. CareFusion has identified a potential patient safety risk with the CareFusion Preoperative Skin Prep Trays containing povidone iodine.

CareFusion Preoperative Skin Prep Trays are medical device convenience kits containing two bottles with PVP-I solutions along with other medical device items such as sponges, gloves, and drapes. Povidone-iodine bottles with loose caps or failed seals may result in PVP-I solution leakage, soiling other components within the kit. Additionally, bottles with loose caps or failed seals may lead to elevated levels of ethylene oxide (EO) sterilant and/or by-products within the PVP-I solution, which may represent a patient safety risk.

This product was distributed January 01, 2011 to present.

Please check your inventory for the above product and lot number. A letter describing the procedure to destroy any affected products will follow via mail to customers who purchased these products in the past.


February 9, 2012


Retail Level Recall



Product:Sodium Chloride 0.9% (NACL)
Moore's Re-order#: 54304
Lot #:Lot# 94-833-KL (Lot number may be followed by 01, 02, or 03)
NDC# 0409-7983-02

Manufacturer:Hospira

PRODUCT SUBJECT TO RECALL

Hospira, Inc. is voluntarily recalling one lot of 0.9% Sodium Chloride Injection, USP due to confirmed out of specification results for in-process chemical assay during lot specific protocol testing.

Please check your inventory for the above products and lot numbers. A letter describing the procedure to return any affected products will follow via mail to customers who purchased these products in the past.


February 9, 2012


Retail Level Recall



Product:Lidocaine with D5W
Moore's Re-order#: 89477
Lot #:92-643-KL (Lot number may be followed by 01, 02, or 03)
NDC# 0409-7931-32

Manufacturer:Hospira

PRODUCT SUBJECT TO RECALL

Hospira, Inc. is voluntarily recalling one lot of 0.4% Lidocaine Hydrochloride and 5% Dextrose Injection, USP, due to confirmed out of specification results for in-process chemical assay during lot specific protocol testing.

Please check your inventory for the above products and lot numbers. A letter describing the procedure to return any affected products will follow via mail to customers who purchased these products in the past.


February 9, 2012


Retail Level Recall



Product:Furosemide Injection USP
Moore's Re-order#: 62984, 90308
Lot #: 85-246-EV (Lot number may be followed by 01)
NDC# 0409-1639-10

Manufacturer:Hospira

PRODUCT SUBJECT TO RECALL

Hospira, Inc. is voluntarily recalling one lot of Furosemide Injection, USP due to confirmed out of specification result at the 18 month testing interval for pH.

Please check your inventory for the above products and lot numbers. A letter describing the procedure to return any affected products will follow via mail to customers who purchased these products in the past.


January 31, 2012


Retail Level Recall



Product:Excedrin Migraine Caplet, Excedrin Migraine Geltab, Excedrin X-Strength Tablets 100's, Excedrin X-Strength Tablets 24's
Moore's Re-order#: 92859, 89661, 92829, 91145
Lot #: All lots w/expiration dated of Dec 20, 2014 or earlier

Manufacturer:Novartis

PRODUCT SUBJECT TO RECALL

Novartis Consumer Healthcare, Inc. is voluntarily recalling all lots of the Excedrin listed above. These recalls are being implemented following consumer complaints of chipped and broken pills and inconsistent bottle packaging line clearance practices at their Lincoln, Nebraska facility, which could result in the bottles containing foreign tablets, caplets or capsules.

Please check your inventory for the above products and lot numbers. A letter describing the procedure to return any affected products will follow via mail to customers who purchased these products in the past.


January 20, 2012


Retail Level Recall



Product:Clinitest HCG Test
Moore's Re-order#: 75569
Lot #:028619, 028924, 029997, 030240, 030431, 030602, 030826, 030998, 031332, 031460, 031662, 031798, 031924, 032106, 032180

Manufacturer:Siemens Healthcare Diagnostics

PRODUCT SUBJECT TO RECALL

Siemens Healthcare Diagnostics is conducting a voluntary recall of CLINITEST hCG Kits because they received complaints associated with borderline or false positive results. Internal testing has confirmed the potential for false positive and increased borderline results with recommended negative quality control materials, as well as patient samples.

This product was shipped starting January 1, 2011 to present.

In Order To Receive Credit You Must:
  • 1. Respond to Moore Medical by February 29, 2012.
  • 2. Provide us with the lot number destroyed.

    If the completed form is received after February 29th or you did not provide us with a lot number, You Will Not Receive Credit.

    Please check your inventory for the above product and lot numbers. A letter describing the procedure to destroy any affected product will follow via mail to customers who purchased this product in the past.


    01/05/2012


    Retail Level Recall



    Product:Kenalog®-40
    Moore's Re-order#: 65261
    Lot #:0L56792

    Manufacturer:Bristol-Myers Squibb

    PRODUCT SUBJECT TO RECALL

    Bristol-Myers Squibb Company is voluntarily recalling the KENALOG Injection lot listed above. This voluntary recall is being conducted as a precautionary measure and is based on the Company's (Bristol-Myers Squibb) investigation of a small number of complaints for difficulty in withdrawal of the listed KENALOG lot from the vial with a syringe and in administering to patients. Their investigation determined that the active ingredient used in the subject lot was of atypical particle size. There have been no efficacy or safety issues reported for the listed KENALOG lot. This product was shipped starting on March 29, 2011 to present. This recall is being conducted to the retail / dispensing level.

    Please check your inventory for the above products and lot numbers. A letter describing the procedure to return any affected products will follow via mail to customers who purchased these products in the past.


    11/9/2011


    Retail Level Recall



    Product:Kenalog®-10
    Moore's Re-order#: 02772
    Lot #:0K65465

    NDC 0003-0494-20

    Manufacturer: Bristol-Myers Squibb

    PRODUCT SUBJECT TO RECALL

    Bristol-Myers Squibb Co is voluntarily recalling KENALOG Injection. This recall is being conducted to the retail/dispensing level with the knowledge of the US Food and Drug Administration and is limited to specific lots and dosages.

    This voluntary recall is being conducted as a precautionary measure and is based on Bristol-Myers Squibb's investigation of a small number of complaints for difficulty in withdrawal of the listed KENALOG lots from the vial with a syringe and in administering to patients. Their investigation determined that the active ingredient used in the subject lots was of atypical particle size. There have been no efficacy or safety issues reported for the listed KENALOG lots.

    This product was shipped starting January 31, 2011 to present.

    Please check your inventory for the above products and lot numbers. A letter describing the procedure to return any affected products will follow via mail to customers who purchased these products in the past.


    11/09/2011


    Retail Level Recall



    Product:Kenalog®-40
    Moore's Re-order#: 02771, 65261
    Lot #:0K66391, 0K666412, 0k66414, 0k66501

    NDC 0003-0293-20, 0003-0293-28

    Manufacturer:Bristol-Myers Squibb

    PRODUCT SUBJECT TO RECALL

    Bristol-Myers Squibb Co is voluntarily recalling KENALOG Injection. This recall is being conducted to the retail/dispensing level with the knowledge of the US Food and Drug Administration and is limited to specific lots and dosages.

    This voluntary recall is being conducted as a precautionary measure and is based on Bristol-Myers Squibb's investigation of a small number of complaints for difficulty in withdrawal of the listed KENALOG lots from the vial with a syringe and in administering to patients. Their investigation determined that the active ingredient used in the subject lots was of atypical particle size. There have been no efficacy or safety issues reported for the listed KENALOG lots.

    This product was shipped starting January 31, 2011 to present.

    Please check your inventory for the above products and lot numbers. A letter describing the procedure to return any affected products will follow via mail to customers who purchased these products in the past.


    10/26/2011


    Retail Level Recall



    Product:Maalox Advanced Maximum Strength Cherry Flavored Liquid 12oz
    Moore's Re-order#: 37790
    Lot #:10105720 Exp. 2/28/13 (NDC 00067025471)

    Manufacturer:Novartis

    PRODUCT SUBJECT TO RECALL

    Novartis Consumer Healthcare, Inc. is voluntarily recalling one lot of the over-the-counter Maalox Advanced Maximum Strength Cherry flavored liquid as a result of an instance of the addition of a small amount of non-USP water (municipal drinking water) during manufacturing.

    Please check your inventory for the above product and lot number. A letter describing the procedure to return any affected products will follow via mail to customers who purchased these products in the past.


    10/24/2011


    Urgent Product Recall



    Product:Povidone Iodine Swabsticks, Solution and Scrub
    Moore's Re-order#: 68549, 68550, 68551, 68552, 68241, 68562, 68563, 68564, 68565, 68566, 68567, 68568, 68569, 68570
    Lot #:Lot #’s – all lots beginning with 8, 9, 0 or 1, followed by a letter A – M (but not I) and followed by two more numbers (example: 9C45). Swabstick lot numbers are located on the packet not on the box.

    Manufacturer:H & P Industries Inc

    PRODUCT SUBJECT TO RECALL

    This recall has been initiated because the products were manufactured without having in place a system for microbial testing at the time of release, without having a system for testing of incoming components, and without having procedures designed and established to prevent objectionable microorganisms in these drug products. The use of these products manufactured under these conditions present a risk of infection in patients undergoing medical and surgical procedures. H & P Industries has not ever received reports of adverse events attributed to these products. This product was shipped September 2008 to present.

    . Please examine your stock immediately to determine if you have any of the above products and lot numbers on hand. If so, discontinue use immediately. Attached to this letter is a Notice of Destruction form issued by H & P Industries. In order to provide you with a credit for affected product that you are destroying (not what you purchased from us), it is imperative that you complete the following steps:

    *1. Verify that you have the affected product. *2. Fill in the company name (Account Name & Number). Account number is required. *3. Fill in the product location (City & State). *4. Destroy the product in one of the manners listed and mark which process was used on the form. *5. Provide information regarding who destroyed / verified the product along with their respective titles. NOTE: These need to be two different people. *6. Fax completed form back to Moore Medical LLC at 866-550-1169. *7. Once we receive your completed form, a credit will be issued to your account in a timely manner.

    Please note Credit will only be issued for products from the affected lots listed above. If you need any additional information, please call our Regulatory Affairs Dept. at 1-800-234-1464 Ext. 5407.


    10/06/2011


    Product Replacement



    Product:Ortho-Glass® Splinting System
    Moore's Re-order#: 82852, 82854
    Lot #:813

    Manufacturer:BSN Medical

    PRODUCT SUBJECT TO RECALL

    It has come to our attention that cartons with an 813 Lot Number sticker were not manufactured by BSN Medical Inc. To determine whether you will need replacement splinting product, please inspect any green and white cartons of ORTHO-GLASS Synthetic Splint System product and locate the lot number. The product in question would have a white sticker on the side of the box with the number “813” on the sticker.

    Please check your inventory for the above products and lot number. A letter describing the procedure to arrange for pick-up and to receive replacement product will follow via mail to customers who purchased these products in the past.


    09/30/2011


    Retail Level Recall



    Product:Alcohol Prep Pads Non Sterile
    Moore's Re-order#: 96640 (NDC# 10819-3912-2)
    Lot #:All lots within product expiry

    Manufacturer:PDI

    PRODUCT SUBJECT TO RECALL

    PDI is voluntarily recalling the non sterile alcohol prep pad due to the potential presence of low levels of a microorganism, BACILLUS CEREUS.

    Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected products will follow via mail to customers who purchased these products in the past.


    09/16/2011


    Retail Level Recall



    Product:HGB Pro Test Strips
    Moore's Re-order#: 86907
    Lot #:Please call 877-881-0710 ext 5407 for a complete list of lot numbers affected

    Manufacturer: ITC

    PRODUCT SUBJECT TO RECALL

    ITC is conducting a voluntary medical device recall for the affected lots, which are listed on the attached table. ITC has determined that results obtained using HgbPro Professional Hemoglobin Test Strips may differ from results obtained using a reference hemoglobin testing system. Testing indicates higher bias from laboratory reference standard than our performance specification of +/-5% or (less than or equal to) 0.5 g/dL.

    A falsely high hemoglobin result may contribute to misdiagnosis of a mildly anemic patient as being "normal". A falsely low hemoglobin result may contribute to misdiagnosis of a patient with a normal hemoglobin concentration as being mildly anemic. Increased risk of inappropriate interventions or delay of an indicated procedure or therapy may result.

    Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected products will follow via mail to customers who purchased these products in the past.


    08/25/2011


    Retail Level Recall



    Product:Cortisporin Otic Solution
    Moore's Re-order#: 00469
    Lot #:A52870C and A52870 (NDC 61570-034-10)

    Manufacturer:King Pharmaceuticals / Monarch Pharmaceuticals

    PRODUCT SUBJECT TO RECALL

    Monarch Pharmaceuticals Inc., a wholly owned subsidiary of Pfizer, Inc. is recalling one lot of Cortisporin Otic Solution. Monarch Pharmaceuticals Inc. voluntarily initiated this recall after stability testing on the lot below produced an out-of-specification potency result for Polymyxin B Sulfate. Please note that administration of the below mentioned lot of Cortisporin Otic Solution is not likely to result in adverse health consequences. This product was shipped starting March 9, 2010.

    Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected products will follow via mail to customers who purchased these products in the past.


    08/25/2011


    Retail Level Recall



    Product:MooreBrand® Mini Blades
    Moore's Re-order#: 81547, 81548
    Lot #:C-051, D-050

    Manufacturer:Pl Medical Co LLC

    PRODUCT SUBJECT TO RECALL

    PL Medical was made aware of a complaint from a Moore Medical customer regarding the use of a Moore Medical #61 mini-blade. The lot number for this complaint is C-051. The customer indicated that they had an issue regarding the cutting-edge of the blade. There is no risk of danger to the patient as a result of the defect. The defect involves only the cutting edge of the blade not being in the correct shape (rounded corners instead of ninety degree angles). Upon further investigation of this lot, PL Medical has determined that they would like to recall the product.

    Please check your inventory for the above product and lot numbers. A letter will be sent to customers who have purchased this product in the past explaining to destroy the product and call Albert Monet at PL Medical (860-243-2100 ext 17) for replacement product. The product SHOULD NOT be returned to Moore Medical.


    07/28/2011


    Recall Notice



    Product:Medline® Pap Smear Kit Tray
    Moore's Re-order#: 81191
    Lot #:All lots starting with 08, 09, 10 followed by a letter (A-Z) in the third position.

    Manufacturer:Medline

    PRODUCT SUBJECT TO RECALL

    This is to inform you that Moore Medical LLC has received a sub-recall notice from Medline Industries, who received a recall notice from Triad Group. The Sterile Lubricating Jelly is being recalled due to concerns regarding the validation of the gamma radiation sterilization cycles for these products. The recall was initiated because use of inadequately sterilized product might result in patient infection.

    Should you have any questions, please call Moore Medical’s Regulatory Affairs Department at 800-234-1464 Ext 5407.


    07/26/2011


    Retail Level Recall



    Product:Sodium Chloride 23.4% Single Dose Vial
    Moore's Re-order#: 51948
    Lot #:Lot# 0362
    NDC# 0517-2930-25

    Manufacturer:American Regent (Luitpold Pharmaceuticals)

    PRODUCT SUBJECT TO RECALL

    This is to notify you that the following lot for the CONCENTRATED SODIUM CHLORIDE INJECTION, USP, 23.4%, NDC# 0517-2930-25 distributed by American Regent, Inc, is the subject of a voluntary recall by Luitpold Pharmaceuticals, Inc., as the manufacturer. This recall was initiated because some of the vials of this lot contain visible particulates.

    Potential adverse events after intravenous administration of solutions containing particulates may include disruption of blood flow within small blood vessels in the lungs, localized inflammation (swelling and accumulation of inflammatory cells), and granuloma formation.

    Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected products will follow via mail to customers who purchased these products in the past.


    May, 24, 2011


    Retail Level Recall



    Product:Skin Prep Protective Barrier
    Moore's Re-order#: 89627
    Lot #:OH266, 0J125, 0J126, 0K118, 0K120, 0L227, 1A246, 1A256

    Manufacturer:Smith & Nephew

    PRODUCT SUBJECT TO RECALL

    Smith & Nephew Inc, Advanced Wound Management Division is voluntarily recalling multiple lot numbers of SKIN-PREP. The decision was made to recall these affected lots after a thorough review of available information regarding conditions at the manufacturing site of the contract manufacturer, H&P Industries dba The Triad Group. It has been determined that the recalled lots were made in the same facility as other wipe products, including wipes, swabs and swab sticks, that are the subject of other voluntary recalls due to a potential contamination issue of these products. This product was shipped January 7, 2010 through present. Testing has been performed on some Smith & Nephew products lots already distributed and/or under quarantine and test results received to date show no contamination. If you have further distributed this product, please inform your customers of this recall.

    Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected products will follow via mail to customers who purchased these products in the past.


    May 24, 2011


    Retail Level Recall



    Product:Thermacare Heat Wrap Menstrual
    Moore's Re-order#: 67994
    Lot #:E06831, NDC# 0573302002

    Manufacturer: Wyeth (Pfizer)

    PRODUCT SUBJECT TO RECALL

    Pfizer Consumer Healthcare (formerly Wyeth Consumer Healthcare) is voluntarily recalling the lot listed below of ThermaCare MENSTRUAL 8HR 3ct Heat Wraps. There is a potential for a leak of the chemical components contained in the heat wrap. This could cause a 2nd degree skin burn (e.g., small red skin blisters or loss of top layer of small area of skin). This product was shipped October 2009 through present. Pfizer Consumer Healthcare (formerly Wyeth Consumer Healthcare) has received 1 report to date of a 2nd degree burn that resulted from leaking products in a wrap from the indentified lot. Approximately 15% of retained samples from the identified lot were found to have the same defect as the reported leaking products so additional burns could occur. If you have distributed any of the affected lot to subaccounts, please notify them of this recall.

    Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected products will follow via mail to customers who purchased these products in the past.


    May 13, 2011


    Recall Flash – Retail Level Recall



    Product:IV Start Kit (contains Triad product)
    Moore's Re-order#: 90196
    Lot #:CZJ03-01, CZJ06-01, CZJ09-01

    Manufacturer:Cypress Medical Products

    PRODUCT SUBJECT TO RECALL

    Cypress Medical Products LLC has received a voluntary product recall notice from Triad Group. The recall involves ALL LOTS of Triad Group Alcohol Prep Pads, Alcohol Swabs and Alcohol Swab Sticks manufactured by Triad Group but which have been private labeled for many accounts and used in procedure trays and convenience kits at other manufacturing companies. This recall involves those Triad Group Alcohol Prep Pads, Alcohol Swabs and Alcohol Swab Sticks marked as Sterile as well as non-sterile. Cypress has proactively held shipments of CYPRESS BRAND IV START KITS after Triad announced a recall on all lots of Alcohol Prep Pads, which are a component of the Cypress Brand IV Start Kits. These products were shipped January 2008 to present.

    Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected products will follow via mail to customers who purchased these products in the past.


    May 13, 2011


    Recall Flash – Retail Level Recall



    Product:Kit Size Alcohol Prep Pad
    Moore's Re-order#: 89579
    Lot #:All lots of Alcohol Prep Pads

    Manufacturer:Certified Safety Mfg Inc

    PRODUCT SUBJECT TO RECALL

    As of January 5, 2011, one of Certified Safety’s vendors, Triad Group, has issued a voluntary recall which includes ALL LOTS of alcohol prep pads produced during calendar year 2010. These prep pads have been packed in a variety of First Aid kits by Certified Safety Mfg during that time frame.

    Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected products will follow via mail to customers who purchased these products in the past.


    May 13, 2011


    Recall Flash – Retail Level Recall



    Product:Urethral Tray
    Moore's Re-order#: 89146, 55239
    Lot #:908528, 909505

    Manufacturer:Cardinal Health

    PRODUCT SUBJECT TO RECALL

    Moore Medical LLC has received a sub-recall notice from Cardinal Health, who received a recall notice from Medikmart, who received a recall notice from Triad Group. The Triad sterile and non-sterile Alcohol Prep Pads, Swabs, and Swab Sticks are being recalled due to concerns regarding potential contamination with bacillus cereus. The recall was initiated because use of these products may potentially lead to a patient infection.

    1. Immediately check your stock for these items. If you have any of these items, the Triad Alcohol component cannot be used. 2. After identifying the affected kits, contact Medikmart at 847-887-8400 so they can send you a sticker to place on the outside of the kit.

    3. Once you receive the sticker, place it on the outside of the kit and instruct your personnel not to use the Triad product contained within. DO NOT use the Triad product, pull another approved product from sterile supply. The prep pads/swabs/swab sticks that are within the kits must be discarded when the caregiver opens the pack.

    4. If you have further distributed these items, please contact your accounts and instruct them to call Medikmart for stickers.

    5. Please fill out the Verification Form identifying the quantity of affected product you have on hand. Return the form regardless if you have any stock.

    Note: By signing and returning the Verification Form you acknowledge that you received and understand this notification.

    Should you have any questions, please call Moore Medical’s Regulatory Affairs department at 800-234-1464 ext 5407.


    May 6, 2011


    RECALL FLASH



    Product: Dermabond Topical Skin Adhesive
    Moore's Re-order#: 79311, 72093, 87429
    Lot #:CJE222, CJP430, CJR302, CJR488, CJR604, CKB001, CKB157, CKB231, CKB492, CKB584, CKB681, CKB820, CKB966, CKE195, CKE335, CKE336, CKE655, CKE842, CKP038, CKP201, CKP358

    Manufacturer:Johnson and Johnson

    PRODUCT SUBJECT TO RECALL

    Ethicon is voluntarily recalling multiple lots of DERMABOND Topical Skin Adhesive based on repors that some units contained discolored product in the vial, and may also have had prolonged setting times.

    Customers who purchased these products from us in the past will be notified by J & J Ethicon. They are instructed to return the product to Stericycle and they will receive a replacement.


    May 6, 2011


    RECALL FLASH



    Product:MooreBrand® Trauma Kit with Litre Flow Oxygen Inhalation, MooreBrand® Basic Trauma Managment Kit, MooreBrand® Rescue Response Kit, MooreBrand® Rescue Response Kit with Disposable Resuscitator, MooreBrand® Refill Kit, Custom BLS Kit, Custom Kit BHP
    Moore's Re-order#: 51961, 53690, 53692, 53693, 53694, 93124, 95595
    Lot #:All lots

    Manufacturer:Triad Group

    PRODUCT SUBJECT TO RECALL

    Moore Medical LLC has received a recall notice from Triad Group that the sterile and non-sterile Alcohol Prep Pads are being recalled due to concerns regarding potential contamination with Bacillus Cereus. The recall was initiated because use of this product may potentially lead to a patient infection.


    04/14/2011


    Recall Flash – Retail Level Recall



    Product:Povidone Iodine Prep Pads Box/100
    Moore's Re-order#: 68548
    Lot #:All lots beginning with the digits 8, 9, 0 or 1 (within their labeled expiration dating)

    Manufacturer:H & P Industries

    PRODUCT SUBJECT TO RECALL

    This is to inform you of a recall involving POVIDONE IODINE PREP PADS, manufactured by H&P Industries, Inc. (distributed by Triad). This recall has been initiated due to concerns expressed by the FDA regarding the potential contamination of these products with an objectionable organism, Elizabethkingia meningoseptica. H&P's internal investigation also concluded a raw material compenent as the potential source of this contamination.

    Please check your inventory for the above product and lot numbers. A letter describing the procedure on how to destroy any affected products will follow via mail to customers who purchased this product in the past.


    04/14/2011


    Recall Flash – Retail Level Recall



    Product:Heparin Lock Flush Syringe 5mL
    Moore's Re-order#: 83393
    Lot #:9082104, 9082114, 9082154, 9092164

    Manufacturer:Covidien

    PRODUCT SUBJECT TO RECALL

    Covidien is conducting this voluntary recall on MONOJECT PREFILL ADVANCED Flush Syringe Containing Heparin in response to a notification received from it's heparin supplier, whose testing showed, that crude heparin used to produce a specific batch of purified heparin sodium USP contained a low level of Over-Sulfated Chondroitin Sulfate (OSCS). Using state of the art testing, the OSCS contaminant was not detectable in the purified heparin sodium USP. However, as a precaution, Covidien is requesting that customers quarantine and return any remaining stock of the lots listed.

    Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected products will follow via mail to customers who purchased these products in the past.


    04/14/2011


    Recall Flash – Retail Level Recall



    Product:Bacteriostatic Sodium Chloride Injection 0.9% USP
    Moore's Re-order#: 77404 (NDC# 0517-0648-25)
    Lot #:9330, 9599, 9828

    Manufacturer:American Regent (Luitpold Pharmaceuticals)

    PRODUCT SUBJECT TO RECALL

    This is to notify you that the lots listed below for the BACTERIOSTATIC SODIUM CHLORIDE INJECTION, USP 0.9% 30mL vials, NDC# 0517-0648-25, distributed by American Regent, Inc., are the subject of a voluntary recall by Luitpold Pharmaceuticals, Inc., as the manufacturer. This voluntary recall was initiated because some of the vials of these lots may contain visible particles.

    Potential adverse events after intravenous administration of solutions containing particulates may include disruption of blood flow within small blood vessels in the lungs, localized inflammation (swelling and accumulation of inflammatory cells), and granuloma formation. American Regent is undertaking this voluntary recall in consideration of the potential for safety issues if these lots of product are administered to patients.

    Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected products will follow via mail to customers who purchased these products in the past.


    04/14/2011


    Recall Flash – Retail Level Recall



    Product:Sodium Chloride 23.4%
    Moore's Re-order#: 51948
    Lot #:9198, 9252, 9299, 9305, 9402, 9423, 9432, 9553

    Manufacturer:American Regent (Luitpold Pharmaceuticals)

    PRODUCT SUBJECT TO RECALL

    This is to notify you that the following lots for the CONCENTRATED SODIUM CHLORIDE INJECTION, USP, 23.4%, 30mL vials, NDC# 0517-2930-25 distributed by American Regent, Inc, is the subject of a voluntary recall by Luitpold Pharmaceuticals, Inc., as the manufacturer. This voluntary recall was initiated because some of the vials of these lots may contain visible particulates.

    Potential adverse events after intravenous administration of solutions containing particulates may include disruption of blood flow within small blood vessels in the lungs, localized inflammation (swelling and accumulation of inflammatory cells), and granuloma formation. American Regent is undertaking this voluntary recall in consideration of the potential for safety issues if these lots of product are administered to patients.

    Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected products will follow via mail to customers who purchased these products in the past.


    04/11/2011


    Retail Level Recall



    Product:Incision/Drainage Pack, IV Start Kit w/Tegaderm, Suture Removal Kit Premium, IV Starter Kit 74030
    Moore's Re-order#: 82764, 82765, 82766, 79446
    Lot #:All lots.

    Manufacturer:Medline Industries

    PRODUCT SUBJECT TO RECALL

    This is to inform you that Moore Medical LLC has received a sub-recall notice from Medline Industries, who received a recall notice from Triad Group. The sterile and non-sterile Alcohol Prep Pads, Swabs, and Swab Sticks are being recalled due to concerns regarding potential contamination with bacillus cereus. The recall was initiated because use of these products may potentially lead to a patient infection.

    Please check your inventory for the above products and lot numbers. A letter describing the procedure on how to handle the affected products will follow via mail to customers who purchased these products in the past.


    04/11/2011


    Retail Level Recall



    Product:Dexamethasone Sodium Phosphate Injection USP
    Moore's Re-order#: 77399, 65977
    Lot #:Lot# see listing for all lot numbers.

    Manufacturer:American Regent

    PRODUCT SUBJECT TO RECALL

    This is to notify you that all unexpired lots, on the attached listing, of Dexamethasone Sodium Phosphate Injection, USP, 4mg/mL, 1mL Single Dose Vial, NDC# 0517-4901-25: 5 mL Multiple Dose Vial, NDC# 0517-4905-25: and 30 mL Multiple Dose Vial, NDC# 0517-4930-25, distributed by American Regent, Inc., are the subject of a voluntary Recall by Luitpold Pharmaceuticals, Inc., as the manufacturer. Recall of this product was initiated because some vials of these lots either contain particulates or have the potential to form particulates prior to their respective expiration dates. Potential adverse events after intravenous administration of solutions containing particulates may include disruption of blood flow within small blood vessels in the lung, localized inflammation (swelling and redness due to accumulation of inflammatory cells), and granuloma formation. Intramuscular administration could result in foreign body inflammatory response, with local pain, swelling and possible long term granuloma formation.

    Please check your inventory for the above products and lot numbers. A letter describing the procedure to return any affected products will follow via mail to customers who purchased these products in the past.


    03/28/2011


    Retail Level Recall



    Product:Amiodarone 50mg/mL Prefilled Syringe
    Moore's Re-order#: 85622
    Lot #:ER001, ER002, ER003, ER004, ER005, ER006, ER007, ER008, ER009, ER010

    Manufacturer:Sagent

    PRODUCT SUBJECT TO RECALL

    Sagent has initiated this voluntary recall due to reports of incompatibility of certain needless I.V. sets with Luer-Activating Devices with Sagent's Amiodarone Pre-filled Syringes, resulting in adverse events. If you may have further distributed this product, please identify those customers and notify them at once of this product recall.

    Please check your inventory for the above products and lot numbers. A letter describing the procedure to return any affected products will follow via mail to customers who purchased these products in the past.


    03/28/2011


    Retail Level Recall (Wholesaler/Reseller Accounts Only)



    Product:Advil 200mg Tabs, 200 Count
    Moore's Re-order#: 81631
    Lot #:D63757

    Manufacturer:Pfizer

    PRODUCT SUBJECT TO RECALL

    Pfizer Consumer Healthcare is recalling the item listed above because testing revealed an out of specification result on the ibuprofen assay value due to overweight tablets that may result in over potency for the bulk lot of the above referenced packaged lot as specified in the New Drug Application (NDA) for Advil Tablets. Please note that administration of the above mentioned lot of Advil Tablets 200 CT is not likely to result in adverse health consequences.

    Please check your inventory for the above products and lot numbers. A letter describing the procedure to return any affected products will follow via mail to customers who purchased these products in the past.


    03/28/2011


    Retail Level Recall



    Product:Epinephrine 0.3mg Auto-Injection
    Moore's Re-order#: 95674, 95675
    Lot #:G100702W, G100801X

    Manufacturer:Greenstone

    PRODUCT SUBJECT TO RECALL

    Greenstone LLC is voluntarily conducting a sub-recall on the below listed lots of Epinephrine Injection, USP (auto-injector) 0.3mg recalled by Shionogi Pharma, Inc. the NDA holder; and manufactured by Phillips Plastics/Hospira. Shionogi's recall notification to Greenstone LLC states that the recall is due to the possibility that a small number of sheaths covering the needles may have pin- holes which my affect sterility.

    Please check your inventory for the above products and lot numbers. A letter describing the procedure to return any affected products will follow via mail to customers who purchased these products in the past.


    03/28/2011


    Retail Level Recall



    Product:Twinject 0.3mg Auto Injection Pkg/2 2pk
    Moore's Re-order#: 86516
    Lot #:U100701B

    Manufacturer:Shionogi Pharma Inc

    PRODUCT SUBJECT TO RECALL

    Shionogi, the NDA holder, is recalling the product and lot number mentioned below because the possibility exists that a small number of sheaths covering the needle may have pinholes. The lots of finished product share a common lot of needle sheaths with auto- injectors produced later that were identified to have a sink developed in the tip area of the needle sheath. The depth of the sink allowed for a small hole to develop in the sheath directly behind the tip location.

    Health Hazard Assessment: While the hole in the needle sheath does represent a breach of sterility, the potential exposure to the needle gauge from substances such as water, dirt particles, chemicals etc is remote due to the configuration of the unit that encases the needle sheath prior to activation and usage during a severe allergic reaction. While there is remote possibility of contamination of the needle with microorganism introduced underneath the skin during administration of the epinephrine during a potentially life-threatening severe allergic reaction; the likelihood of this contamination occurring and thereby causing significant health consequences to the general population and the immune-compromised population is not likely.

    Please check your inventory for the above products and lot numbers. A letter describing the procedure to return any affected products will follow via mail to customers who purchased these products in the past.


    02/07/2011


    Recall Flash – Retail Level Recall



    Product:SALT Airway Tube
    Moore's Re-order#: 99534
    Lot #:C10259, D103334

    Manufacturer:Microtek Medical

    PRODUCT SUBJECT TO RECALL

    This recall has been initiated in response to a notification by Triad Group in regards to the sterilization validation of the gamma radiation sterilization cycles utilized for the processing of the Sterile Lubricating Jelly contained with the S.A. L. T. Airway Device (79-580). Triad Group has indicated that the use of inadequately sterilized product might result in patient infection.

    Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected product will follow via mail to customers who purchased this product in the past.


    01/27/2011


    Recall Flash – Retail Level Recall



    Product:Sodium Bicarbonate Injection USP .5%, 3.75grams, 44.6mEq/50mL
    Moore's Re-order#: 78189
    Lot #:8833, 9130, 9342, 9543, 9702, 0068, 0276, 0581, 0745

    Manufacturer:American Regent

    PRODUCT SUBJECT TO RECALL

    This voluntary recall was initiated because some vials of these lots contain particulates. Potential adverse events after intravenous administration include damage to blood vessels in the lung, localized swelling, and granuloma formation.

    Please check your inventory for the above products and lot numbers. A letter describing the procedure to return any affected products will follow via mail to customers who purchased these products in the past.


    01/27/2011


    Recall Flash – Retail Level Recall



    Product:Sodium Bicarbonate Injection USP 8.4% (50mEq)
    Moore's Re-order#: 52414
    Lot #:8845, 9062, 9058, 9111, 9128, 9158, 9180, 9212, 9262, 9271, 9292, 9346, 9346A, 9360, 9374, 9396, 9412, 9438, 9720, 9801, 9821, 0054, 0115, 0162, 0172, 0237, 0427, 0528, 0597, 0649

    Manufacturer:American Regent

    PRODUCT SUBJECT TO RECALL

    This voluntary recall was initiated because some vials of these lots contain particulates. Potential adverse events after intravenous administration include damage to blood vessels in the lung, localized swelling, and granuloma formation.

    Please check your inventory for the above products and lot numbers. A letter describing the procedure to return any affected products will follow via mail to customers who purchased these products in the past.


    01/24/2011


    Recall Flash – Retail Level Recall



    Product:Alcohol Prep Pads (Moore Brand & Triad)
    Moore's Re-order#: 68533, 68534, 68537, 68538, 68540, 68541, 76141, 88425
    Lot #:All

    Manufacturer:Triad

    PRODUCT SUBJECT TO RECALL

    This recall has been initiated due to concerns from a customer about potential contamination of the products with an objectionable organism that may or may not be related to Triad’s manufacture of these products. Out of an abundance of caution, Triad is recalling these lots and revalidating their production lines to ensure that they are not the source of these contamination issues.

    Please check your inventory for the above products. A letter describing the procedure on how to properly destroy any affected products will follow via mail to customers who purchased these products in the past.


    01/18/2011


    Flash – Retail Level Recall



    Product:Vacutainer Push Button Blood Collection Set
    Moore's Re-order#: 75337
    Lot #:0145457, 0152300, 0153981, 0153982, 0158081, 0158082, 0158084, 0160664, 0160666, 0165202, 0165205, 0165207, 0165218, 0165226, 0165227, 0165232, 0165234, 0176872, 0179208, 0179209, 0179212, 0180023, 0180026, 0180027, 0180028, 0180040, 0180042, 0196209, 0196210, 0201399, 0201400, 0201402, 0208593, 0211641

    Manufacturer:BD

    PRODUCT SUBJECT TO RECALL

    BD is recalling the above referenced product and lot numbers because of concerns that some products may demonstrate a problem that could cause the IV cannula to separate from the hub during the venipuncture process.

    Please check your inventory for the above product and lot numbers. A letter describing the procedure to return the affected product to BD for replacement will follow via mail to customers who purchased this product in the past. The customer SHOULD NOT return the product to Moore Medical LLC.


    01/12/2011


    Recall Flash – Retail Level Recall



    Product:Lubricating Jelly
    Moore's Re-order#: 68572, 68573, 75774, 76134, 94087, 68574
    Lot #:Beginning with 7, 8, 9 or 0 (within labeled expiration dating)

    Manufacturer:Triad

    PRODUCT SUBJECT TO RECALL

    This recall has been initiated due to concerns expressed by the Food and Drug Administration regarding the validation of the gamma radiation sterilization cycles for these products. Triad is initiating this recall because use of inadequately sterilized product might result in patient infection.

    Please check your inventory for the above products. A letter describing the procedure on how to properly destroy any affected products will follow via mail to customers who purchased these products in the past.


    01/12/2011


    Recall Flash – Retail Level Recall



    Product:Steril-Eyes Eye Wash B/A Free
    Moore's Re-order#: 85511
    Lot #:W09801SE, W09802SE, W09804SE

    Manufacturer:Water Jel

    PRODUCT SUBJECT TO RECALL

    Water Jel has initiated this recall due to GMP violations and issues with the manufacturer of this product.

    Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected product will follow via mail to customers who purchased this product in the past.


    01/12/2011


    Flash – Retail Level Recall



    Product:Dexamethasone Sodium Phosphate Injection USP
    Moore's Re-order#: 59188
    Lot #:8811, 9093, 9195, 9296, 9419, 9505, 9649

    Manufacturer:American Regent

    PRODUCT SUBJECT TO RECALL

    The recall of this product was initiated because some vials of these lots either contain particulates or have the potential to form particulates prior to their respective expiration dates.

    Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affected product will follow via mail to customers who purchased this product in the past.


    01/12/2011


    Recall Flash – Retail Level Recall



    Product:Athletic Supporter
    Moore's Re-order#: 92935, 92115
    Lot #:All Lots

    Manufacturer:Scott Specialties

    PRODUCT SUBJECT TO RECALL

    Scott Specialties has initiated this recall because they have recently discovered that the SA1503 athletic supporter has some elastic components which contain latex. While the latex elastimer is completely covered in fabric, and as such, should be of little or no risk, the product is labeled as “latex free”.

    Please check your inventory for the above products and lot numbers. A letter describing the procedure to return any affected products will follow via mail to customers who purchased these products in the past.


    01/05/2011


    Recall Flash – Retail Level Recall



    Product:Precision Xtra Test Strips
    Moore's Re-order#: 68913, 79727, 88641, 93002, 88224
    Lot #:Various

    Manufacturer:Abbott

    PRODUCT SUBJECT TO RECALL

    Abbott Diabetes Care is recalling certain lots of Precision Xtra, Optium, OptiumEZ and Precision Point of Care Blood Glucose Test Strips because the strips may generate erroneously low blood glucose results. Erroneously low results that are not recognized may pose significant risks to your health.

    The test strips are used with Abbott’s Precision Xtra, Precision Xceed Pro, MediSense Optium, Optium and OptiumEZ blood glucose monitoring systems. The blood glucose monitors are not being recalled and customers can continue to use the blood glucose monitors.

    Please check your inventory for the above products and lot numbers. A letter describing the procedure to return any affected products will follow via mail to customers who purchased these products in the past.


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