June 7, 2010
Recall Flash – Retail Level Recall
Product:Tylenol Infant Suspension
Moore's Re-order#: 89028
Lot #:All lots that have not yet expired
Manufacturer:McNeil Consumer Healthcare
PRODUCT SUBJECT TO RECALL
McNeil Consumer Healthcare is initiating this voluntary recall because some of these products may not meet required quality standards. Some of the products may contain a higher concentration of active ingredient than is specified; others may contain inactive ingredients that may not meet internal testing requirements; and others may contain tiny particles. While the potential for serious medical events is remote, McNeil advises consumers who have purchased these recalled products to discontinue use.
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.
DATE: May 12, 2010
Recall Flash – Retail Level Recall
Product:Tylenol Child Liq 4oz
Tylenol Child Susp Grape 4oz
Tylenol Child Liq 4oz
Children’s Motrin Liq Berry 4oz
Motrin Child Susp 4oz
Benadryl Child Liq 4oz
Moore's Re-order#: 88755, 90765, 88854, 51881, 90169, 88853
Lot #:All lots that have not yet expired
Manufacturer:McNeil Consumer Healthcare
PRODUCT SUBJECT TO RECALL
McNeil Consumer Healthcare is initiating this voluntary recall because some of these products may not meet required quality standards. Some of the products may contain a higher concentration of active ingredient than is specified; others may contain inactive ingredients that may not meet internal testing requirements; and others may contain tiny particles. While the potential for serious medical events is remote, McNeil advises consumers who have purchased these recalled products to discontinue use.
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 19, 2010
Recall Flash – Retail Level Recall
Product:Tylenol Extra Strength Caplets Btl/24, Tylenol Extra Strength Caplets Btl/100, Rolaids Multi-Sympton Berry Btl/100, Tylenol 8 Hour Caplet Btl/100
Moore's Re-order#: 17469, 17471, 73517, 79791
Lot #:Various
Manufacturer:J & J / McNeil Consumer Healthcare
PRODUCT SUBJECT TO RECALL
J & J / McNeil Consumer Healthcare is initiating this voluntary recall following an investigation of consumer reports of an unusual moldy, musty, or mildew-like odor that, in a small number of cases, was associated with temporary and non-serious gastrointestinal events. These include nausea, stomach pain, vomiting, or diarrhea.
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.
October 23, 2009
Recall Flash – Retail Level Recall
Product:Propofol (10mg/mL, 20mL & 10mg/mL, 50mL)
Moore's Re-order#: 81464, 88089
Lot #:79-814-DJ, 79-816-DJ, 79-817-DJ, 79-818-DJ, 79-820-DJ, 79-821-DJ, 79-823-DJ, 79-824-DJ, 79-825-DJ, 79-827-DJ, 79-872-DJ, 80-006-DJ, 80-009-DJ, 80-011-DJ, 80-012-DJ, 80-016-DJ, 80-017-DJ, 80-020-DJ, 80-021-DJ, 80-022-DJ, 80-025-DJ, 80-026-DJ, 80-028-DJ, 80-103-DJ, 80-104-DJ, 80-108-DJ
Manufacturer:Hospira
PRODUCT SUBJECT TO RECALL
Hospira has initiated this voluntary recall because some of the containers may contain particulate matter. The source of the particulate matter has been identified by Hospira as stainless steel equipment used in the manufacturing process. Hospira has not received any reports of adverse events from its customers. The risk evaluation performed by Hospira’s medical staff has categorized the overall risk as moderate. This recall is being conducted as a precautionary measure. Hospira has identified the root cause and corrective actions have been implemented. Please do not return the product to Moore Medical.
October 28, 2009
Recall Flash – Retail Level Recall
Product:Wallach Surgical Devices
Moore's Re-order#: 62790, 85696, 85705, 85707, 85710
Lot #:900002, 900002A-CO2, 900506-1-CO2, 900506-2-CO2, 900509-5
Manufacturer:Wallach Surgical
PRODUCT SUBJECT TO RECALL
Moore Medical LLC has been notified by Wallach Surgical Devices of a Retail Level recall on the following products. Multi-Tip CO2 Connection, Cryosurgical LL100 CO2 3 tip, WA1000B 900506-1-CO2, Cryosurgical System, Console CO2.
As a result of internal confirmation testing of the Wallach Surgical LL100 Cryosurgery Device and related CO2 Devices, a manufacturing problem has been detected where under certain circumstances a restriction of the flow of carbon dioxide gas within the handle may result in a less than optimum temperature delivery to the treatment site. You will be notified and instructed to contact Wallach Surgical Devices for arrangements to repair or replace the device – at Wallach Surgical’s expense including shipment. Please do not return these items to Moore Medical.
August 28, 2009
Recall Flash – Retail Level Recall
Product:Pedi-Cap CO2 Detector
Moore's Re-order#: 56339
Lot #:Numerous Lot Numbers
Manufacturer:Covidien/Nellcor Puritan Bennett
PRODUCT SUBJECT TO RECALL
Covidien/Nellcor Puritan Bennett has informed us of an urgent voluntary medical device recall because they
received a customer report in which they experienced difficulty manually ventilating an intubated patient through
the PediCap. They believe that a recent modification to the PediCap End-Tidal CO2 Detector may result in
increased resistance to airflow through the PediCap. This could result in ineffective ventilation of the patient
and/or inadequate detection of CO2 levels, so that the indicator paper will not change color.
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.
June 9, 2009
Recall Flash – Retail Level Recall
Product:Assorted Oxygen Supplies
Moore's Re-order#: 51045
51046
51047
51961
51964
Lot #:08-05-3B and 09-01-1B
08-05-3B and 09-01-1B
08-05-3B and 09-01-1B
08-05-3B and 09-01-1B
08-05-3B and 09-01-1B
Manufacturer:Allied Healthcare Products / InterMed Gas Products
PRODUCT SUBJECT TO RECALL
An Allied Healthcare Products supplier, InterMed Gas Products, has initiated a product recall for medical valves. Some of the valves were supplied to Allied and a few were then distributed to Allied customers as Oxygen Cylinder Post Valves, before Allied received the notification from InterMed. InterMed determined that the medical valves in two batches do not meet their quality specifications, which may cause the valve to fail and result in uncontrolled release of oxygen when the valve is in the open position. The batch / lot numbers are clearly visible on the side of the Oxygen Cylinder Post Valves.
Please check your inventory for the above products and lot numbers. A letter describing the procedure to return any affected product will follow via mail to customers who purchased these products in the past. Replacements will be sent to the customer.
June 8, 2009
Recall Flash – Retail Level Recall
Product:R2 Pediatric Triangle Electrodes
Moore's Re-order#: 73832
Lot #: 0810211
Manufacturer: ConMed Corporation
PRODUCT SUBJECT TO RECALL
ConMed has initiated this recall to notify us of a labeling error on the pink pouch of the R2 Multifunction pediatric electrodes (defib pads). These are pediatric defib pads in PINK pouches with WHITE labels attached. The pouch is correct and the product in the pouch is the pediatric product REF# 3200-1711. The WHITE label maybe printed with the information identifying these devices as an R2 ADULT Multifunction electrodes REF# 3111-1721 pads. While it is believed that only a few pouches in the suspect lot bears the incorrect label, the entire lot in question is being recalled.
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.
April 14, 2009
Recall Flash – Retail Level Recall
Product:Allscripts Digoxin Tablets 0.25mg
Moore's Re-order#: 80457
Lot #:9023045, 8350165, 8325065, 8294169, 8291068, 8086157, 8045070, 7334139, 7218363
Manufacturer:A-S Medication Solutions LLC
PRODUCT SUBJECT TO RECALL
Caraco Pharmaceuticals recalled ALL lots within expiry of Digoxin 0.25mg and has notified Allscripts/A-S Medication Solutions of them. The tablets are being recalled because they may differ in size and therefore could have more or less of the active ingredient, Digoxin. Caraco is recalling these tablets to minimize any potential risk to patients. These lots were distributed by A-S Medication Solutions under A-S Medication Part# 5758-0.
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.
April 2, 2009
Recall Flash – Retail Level Recall
Product:Ultrasite IV Admin Set
Moore's Re-order#: 86398
Lot #:61028769, 61028767, 61028771, 61028772, 61028766, 61028765, 61028764, 61028763, 61028761, 61028762
Manufacturer:B Braun
PRODUCT SUBJECT TO RECALL
B Braun has elected to initiate a voluntary product removal of the above products and lot numbers. They have received reports of occlusion/no flow issues due to an identified issue with a purchased component contained in the above products. While the issue of occlusion/no flow renders the IV set unusable and a new set needs to be obtained, the risk to the patient is negligible.
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.
April 2, 2009
Recall Flash – Retail Level Recall
Product:ULTRASITE B Series ADDitIV Primary Administration Set
Moore's Re-order#: 69421
Lot #:61030997, 61031000, 61031001, 61031002, 61031004
Manufacturer:B Braun
PRODUCT SUBJECT TO RECALL
B Braun has elected to initiate a voluntary product removal of the above products and lot numbers. They have received reports of occlusion/no flow issues due to an identified issue with a purchased component contained in the above products. While the issue of occlusion/no flow renders the IV set unusable and a new set needs to be obtained, the risk to the patient is negligible.
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.
December 26, 2008
Recall Flash – Retail Level Recall
Product:Intravenous Pump FLO-GARD
Moore's Re-order#: 73749
Lot #:PRODUCT CODE: 2M8063
Manufacturer:Baxter
PRODUCT SUBJECT TO RECALL
Baxter is voluntarily recalling the above lots because they have identified that during the normal course of use or transport, a cable connecting the internal circuit board to the keypad may become dislodged, affecting keypad operability. A review of complaint data over the past five years shows no reports of injuries related to this issue.
Please check your inventory for the above product and lot number. A letter describing the procedure on how to handle the affected product will follow via mail to customers who purchased these products in the past.
12/15/2008
Recall Flash – Retail Level Recall
Product:Promethazine 25mg/mL
Moore's Re-order#: 70539
Lot #: 070215, 070217, 080525
Manufacturer: Bioniche Pharma
PRODUCT SUBJECT TO RECALL
Bioniche Pharma is voluntarily recalling the above lot numbers. They have decided to take this action following an investigation indicating increased and out of specification levels of a known degradant of Promethazine in two of the lots. Recall of the third lot is precautionary. There have been no complaints or adverse events reported for the affected lots.
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.
November 17, 2008
Recall Flash – Retail Level Recall
Product:Coloscreen
Moore's Re-order#: 16424, 16427, 16426, 16425
Lot #:14-06, 1-07, 3-07, 4-07, 5-07, 6-07, 8-07
5-06, 6-06, 7-06, 1-07, 2-07, 3-07
2-07, 3-07, 5-07
5-06, 6-06, 1-07, 2-07, 3-07, 4-07
Manufacturer:Helena Laboratories
PRODUCT SUBJECT TO RECALL
Helena Laboratories has become aware that certain lots of fecal occult blood test developer shipped in 2006 and 2007 may have undergone degradation during extended storage. This degradation does not affect the published test sensitivity or patient result. However, it could produce weak (faint blue) or no development on the positive monitor on some guaiac FOBT slides. All developer(s) have expiration dates from June 2009 to April 2010.
Please check your inventory for the above products and lot numbers. Helena Laboratories will be sending letters to our customers, who have purchased these in the past, describing the procedure on how to handle the affected products. Just the developer is being replaced not the whole kit.
November 5, 2008
Recall Flash – Retail Level Recall
Product:R2 Multifunction Electrodes
Moore's Re-order#: 73838, 73839
Lot #:0808051, 0808011, 0808041, 0808121
Manufacturer:ConMed Corporation
PRODUCT SUBJECT TO RECALL
ConMed Corporation is urgently notifying us of a label color error on the pouch of the R2 Multifunction electrodes (defib pads). In an attempt to enable customers to quickly identify each pad that connects to a specific type of defibrillator, ConMed color coded the labels on the pouches of the R2 Multifunction defib pads. They found that pouches requiring a green label were labeled using peach label stock. While the information printed on the label is correct, the color choice of the label stock was wrong. ConMed has not received any reports of end users having a problem identifying these devices.
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
October 1, 2008
Recall Flash – Retail Level Recall
Product:Fluro-Ethyl Mist
Moore's Re-order#: 65570
Lot #:7010, 7011 and 7012
Manufacturer:Gebauer Company
PRODUCT SUBJECT TO RECALL
Gebauer Company is conducting a voluntary recall on these lot numbers because they may contain some units with a defective valve. Units of Gebauer’s Fluro-Ethyl containing the defective valve could malfunction and spray out from the valve when the product is actuated. While Gebauer has received no reports of an injury associated with these three lots, there is a potential risk that a malfunctioning unit could inadvertently spray a healthcare provider or patient and cause an injury to the eye.
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 these products in the past.
September 29, 2009
Recall Flash – Retail Level Recall
Product:Nylon Sutures
Moore's Re-order#: 44625
Lot #:M335780
Manufacturer:Surgical Specialties
PRODUCT SUBJECT TO RECALL
Surgical Specialties Corporation dba Angiotech is recalling the above mentioned product with the lot number listed above because there is a possibility that lot M335780 of item code 925B may contain mixed product. The box and pouch labels reference 3-0 Black Mono Nylon with a C7 needle, item code 925B. When pouches are opened, the inner card may be labeled as a size 4-0 and the suture material will be 4-0 Black Braided Silk with a C6 needle.
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.
August 27, 2008
Recall Flash – Retail Level Recall
Product:Vicryl Rapide Suture VR214 and VR426
Moore's Re-order#: 55319, 55322
Lot #:ZG9CJXD0, ZG8BTSD0, ZG9BSPE0
Manufacturer:Johnson & Johnson Ethicon
PRODUCT SUBJECT TO RECALL
Ethicon has initiated a voluntary recall due to a defect in the packaging of select suture lots produced during May-June 2007. There is a potential that the defect could compromise the integrity of the primary seal which could lead to premature suture degradation and/or impair the sterile barrier of the product.
Please check your inventory for the above products and lot numbers. A letter describing the procedure to return any affect products will follow via mail to customers who purchased these products in the past.
August 28, 2008
Recall Flash – Retail Level Recall
Product:Procainamide 100mg/mL 10mL
Moore's Re-order#: 75167
Lot #:48-193-EV
Manufacturer:Hospira
PRODUCT SUBJECT TO RECALL
Hospira is initiating this voluntary recall due to reports of discoloration of the solution ranging from dark yellow to dark amber. Hospira has not received any reports of adverse health events related to this issue. An investigation is ongoing to determine corrective and/or preventative actions.
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.
August 18, 2008
Recall Flash – Retail Level Recall
Product:Cyanide Antidote Kit
Moore's Re-order#: 64238
Lot #:51267, 61477, 81207, 81507, 91257, 91267, 91397, 121417, 31248, 61258
Manufacturer:Akorn
PRODUCT SUBJECT TO RECALL
Akorn was notified by BD of the recall on the BD 60mL Syringe. BD has emphasized that this syringe product may be affected specifically when transported at altitudes associated with air freight delivery (at reduced atmospheric pressures), such that syringe packaging integrity (and therefore BD product sterility) may be impacted.
Please check your inventory for the above product and lot numbers. A letter describing the procedure to return any affect products will follow via mail to customers who purchased these products in the past.
May 15, 2008
Recall Flash – Retail Level Recall
Product:Multi Vita Bets with 1.0mg Fluoride
Moore's Re-order#: 58353, 58354
Lot #:Numerous
Manufacturer:Actavis
PRODUCT SUBJECT TO RECALL
Actavis is recalling the above lot numbers due to out-of-specification results for assay at the stability time-point.
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 this product in the past.
DATE: July 19, 2008
Recall Flash – Retail Level Recall
Product:Metriset Burette Auto Shut Off
Moore's Re-order#: 82705
Lot #:60999544
Manufacturer:B Braun
PRODUCT SUBJECT TO RECALL
B Braun is initiating this voluntary recall of the above product and lot number because it has identified that in a small percentage of burette sets, the injection site at the top of the burette chamber may be missing, thereby leaving an open port.
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.
July 17, 2008
Recall Flash – Retail Level Recall
Product:Phenazopyridine 100mg SC Red Tablet, Phenazopyridine 200mg SC Tablet, Meclizine 25mg Chewable, Prenatal RX Tablet, Prenatal Plus 27mg Iron Tablet
Moore's Re-order#: 58346, 58347, 58360, 58765, 58766
Lot #:All Non Expired Lots
Manufacturer:Actavis
PRODUCT SUBJECT TO RECALL
Actavis is recalling the above products due to lack of stability indicating methods.
Please check your inventory for the above products. A letter describing the procedure to return any affected products will follow via mail to customers who purchased this product in the past.
June 17, 2008
Recall Flash – Retail Level Recall
Product:Amenities Kit
Moore's Re-order#: 84321
Lot #:Mouthwash with code HDX
Manufacturer:Medline Industries
PRODUCT SUBJECT TO RECALL
Medline Industries received a voluntary Market Withdrawal notification from Hyrdox Laboratories, regarding contamination of mouthwash. Medline Industries is recalling the above Amenities Kit that contains mouthwash manufactured by Hydrox. Please check the manufacturer identification code on your product. The code is a series of numbers and letters. If the code contains the letters HDX the product was manufactured by Hydrox.
Please check your inventory for the above product. A letter describing the procedure to return any affected product will follow via mail to customers who purchased this product in the past. The entire kit will need to be returned to receive proper credit.
June 17, 2008
Recall Flash – Retail Level Recall
Product:Heparin Sodium Injection 5000u/mL 1mL Vial
Moore's Re-order#: 82216
Lot #:All
Manufacturer:by Baxter Healthcare
PRODUCT SUBJECT TO RECALL
We have been notified by Baxter Healthcare of a Retail Level recall on the following products.
This item was skipped on the original recall dated 02/29/08.
Baxter Healthcare is expanding its voluntary recall of Heparin Sodium Infection to include all lots of single and multi-dose vial products, due to an increase in reports of adverse patient reactions including abdominal pain, burning sensation, chest pain, diarrhea, dizziness, drug ineffectiveness, dyspepsia, dyspnea, erythema, flushing, headache, hyperhidrosis, hypoesthesia, hypotension, including profound and refactory hypotention, increased lacrimation, loss of consciousness, malaise, nausea, pallor, palpitations, paresthesia, paresthesia (oral), pharyngeal edema, restlessness, vomiting/retching, stomach discomfort, tachycardia, thirst, trismus, and unresponsiveness to stimuli.
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.
June 17, 2008
Recall Flash – Retail Level Recall
Product: Methylprednisolone Acetate
Moore's Re-order#: 77587, 83772
Lot #: 07J704, 07K702
Manufacturer: Teva Pharmaceuticals
PRODUCT SUBJECT TO RECALL
Teva Pharmaceuticals is voluntarily recalling the above lots due to a lack of sterility assurance.
Please check your inventory for the above product and lot numbers. A letter describing the procedure on how to handle the affected product will follow via mail to customers who purchased these products in the past.
May 14, 2008
Recall Flash – Retail Level Recall
Product:Multi Vita-Bets with Fluoride Chewable Tablets
Moore's Re-order#: 58350
Lot #:Numerous
Manufacturer:Actavis
PRODUCT SUBJECT TO RECALL
Actavis is recalling the above lot numbers due to out-of-specification results obtained for assay on stability.
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 this product in the past.
April 14, 2008
Recall Flash – Retail Level Recall
Product:Clinitest HCG Test
Moore's Re-order#: 75569
Lot #: 97552 and 97574
Manufacturer: Siemens
PRODUCT SUBJECT TO RECALL
Siemens Healthcare Diagnostics has identified a potential issue with the above lots. Investigation indicates that the sensitivity of the reagent with Clinitest hCG lots 97552 and 97574 has decreased. This decrease in sensitivity has the potential to generate false negative hCG results. Shelf life of the product is also impacted by the shift in sensitivity and can no longer be guaranteed.
Please check your inventory for the above product and lot numbers. A letter describing the procedure on how to handle the affected product will follow via mail to customers who purchased these products in the past.
April 15, 2008
Recall Flash – Retail Level Recall
Product:Clearview HIV 1/2 Control Kit
Moore's Re-order#: 84406
Lot #:7A322
Manufacturer:Inverness Medical/Chembio
PRODUCT SUBJECT TO RECALL
Inverness Medical / Chemio is recalling the above lot number because recent internal testing has shown that the Clearview HIV Rapid Test Control Pack may result in a false negative interpretation.
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.
April 9,2008
Flash – Retail Level Recall
Product: Heparin Lock Flush Syringe 5mL
Moore's Re-order#: 83393
Lot #:7041194, 7072054, 7113104, 7041204, 7072064, 7113114, 7051534, 7072154, 7113154, 7051544, 7082284, 8010064, 7051554, 7102804, 8010114, 7071924, 7113034, 8010134, 7072034, 7113044, 8010174,
7072044, 7113054
Manufacturer: Kendall Healthcare Products/Tyco Healthcare
PRODUCT SUBJECT TO RECALL
Kendall Healthcare Products / Tyco Healthcare is conducting a voluntary recall of specific lots of Monoject Prefilled syringes which contain heparin. This recall is being conducted due to a notification Tyco Healthcare received from its supplier, Scientific Protein Laboratories (SPL), of a nationwide recall of Heparin Sodium, USP Active Pharmaceutical Ingredient (API).
This recall has been prompted due to a heparin-like contaminant discovered in two lots of API, Tyco Healthcare received from SPL. As indicated by the supplier SPL, typical symptoms may include anaphylactic-like reactions such as low blood pressure, shortness of breath, nausea, vomiting, diarrhea and abdominal pain.
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.
March 6, 2008
Flash – Retail Level Recall
Product:Heparin Sodium Injection
Moore's Re-order#: 77418, 77417
Lot #:All
Manufacturer:Baxter Healthcare
PRODUCT SUBJECT TO RECALL
We have been notified by Baxter Healthcare of a Retail Level recall on the following products.
These are additional lot numbers that were added to the original recall dated 01/17/08.
Baxter Healthcare is expanding its voluntary recall of Heparin Sodium (1000 units 30mL and 5000 units 10mL) Injection to include all lots of single and multi-dose vial products, due to an increase in reports of adverse patient reactions including abdominal pain, burning sensation, chest pain, diarrhea, dizziness, drug ineffectiveness, dyspepsia, dyspnea, erythema, flushing, headache, hyperhidrosis, hypoesthesia, hypotension, including profound and refactory hypotention, increased lacrimation, loss of consciousness, malaise, nausea, pallor, palpitations, paresthesia, paresthesia (oral), pharyngeal edema, restlessness, vomiting/retching, stomach discomfort, tachycardia, thirst, trismus, and unresponsiveness to stimuli.
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.
March 6, 2008
Recall Flash – Retail Level Recall
Product:Hep-Lock 100u 10mL MDV
Moore's Re-order#: 77419
Lot #:All
Manufacturer:Baxter Healthcare
PRODUCT SUBJECT TO RECALL
Baxter Healthcare is voluntarily recalling Baxter Heparin products to include all lots of HEP-LOCK (Heparin Lock Flush Solution, USP) and HEP-LOCK U/P (Preservative-Free Heparin Lock Flush Solution, USP) products.
These products utilize the same active pharmaceutical ingredient (API) source as the recalled Baxter Heparin Sodium for injection single and multi-dose vial products.
Reports of adverse events have been associated with the multi-dose products, and Baxter is taking the precautionary step of recalling all remaining heparin flush products that are currently on the market. While the API has not been implicated as the cause of these increased adverse events, Baxter is recalling all products utilizing this API source.
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 19, 2008
Recall Flash – Retail Level Recall
Product:Nystatin Cream 15gm, 30gm
Moore's Re-order#: 80473, 77716
Lot #:T029, T682, T092, U467, W034, T761, U468
Manufacturer:E Fougera & Company
PRODUCT SUBJECT TO RECALL
E Fougera & Company/Altana is voluntarily recalling the above products and lot numbers because of an out-of-specification stability test result (for potency).
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 29, 2008
Recall Flash – Retail Level Recall
Product:Saline Flush Syringe/Sodium Chloride
Moore's Re-order#: 82913, 82914, 82915, 83882
Lot #:All
Manufacturer: B Braun
PRODUCT SUBJECT TO RECALL
B Braun is initiating this voluntary recall of the above products and lot numbers because it has been determined that there is a potential for the sterility of these lots to be compromised, which may result in potential contamination. This issue may result in patient injury.
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 22, 2008
Recall Flash – Retail Level Recall
Product:Heparin Sodium Injection 1000 Units 10mL & 30mL
Moore's Re-order#: 77418
Lot #:107054, 117085, 047056, 097081, 107024, 107064, 107066, 107074, 107111
Manufacturer: Baxter Healthcare
PRODUCT SUBJECT TO RECALL
Baxter Healthcare is performing a voluntary recall of the above lots of Heparin as a precaution due to an increase in reports of adverse patient reactions including abdominal pain, abdominal pain (upper), decreased blood pressure, burning sensation, chest pain, diarrhea, dizziness, drug ineffectiveness, dyspepsia, dyspnea, erythema, flushing, headache, hyperhidrosis, hypoesthesia, hypotension, lacrimation increased, loss of consciousness, malaise, nausea, pallor, palpitations, paresthesia, paresthesia (oral), pharyngeal edema, restlessness, vomiting/retching, stomach discomfort, tachycardia, thirst, trismus, and unresponsiveness to stimuli. Baxter Healthcare has received no reports involving fatality.
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 11, 2008
Recall Flash – Retail Level Recall
Product: Comvax .5ml Vial SOI-H
Moore's Re-order#: 56244
Lot #: 0376U, 0377U
Manufacturer: Merck
PRODUCT SUBJECT TO RECALL
Merck is taking this voluntary action due to the fact that they can not assure sterility for these specific vaccine lots. In routine testing of the vaccine manufacturing equipment, Merck identified an issue that creates the potential for microorganisms to survive the sterilization process. Merck identified the presence of Bacillus cereus. Sterility tests of the vaccine lots themselves have not found any contamination. The potential for contamination of any individual vaccine is low, and, if present, the level of contamination would be low.
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 11, 2008
Recall Flash – Retail Level Recall
Product: Pedvax HIB SOI-B
Moore's Re-order#: 68715
Lot #:0677U, 0820U, 0995U, 1164U, 0259U, 0435U,
0436U, 0437U, 0819U, 1167U
Manufacturer: Merck
PRODUCT SUBJECT TO RECALL
Merck is taking this voluntary action due to the fact that they can not assure sterility for these specific vaccine lots. In routine testing of the vaccine manufacturing equipment, Merck identified an issue that creates the potential for microorganisms to survive the sterilization process. Merck identified the presence of Bacillus cereus. Sterility tests of the vaccine lots themselves have not found any contamination. The potential for contamination of any individual vaccine is low, and, if present, the level of contamination would be low.
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.
December 28, 2007
Recall Flash – Retail Level Recall
Product:First Aid Kit Soft Sided 81 Piece
Moore's Re-order#: 83322
Lot #: D0047
Manufacturer: First Aid Only
PRODUCT SUBJECT TO RECALL
First Aid Only, Inc. is conducting a voluntary recall of First Aid Only branded first aid kits and/or refills with the lot numbers listed above. These first aid kits and/or refills contain ibuprofen tablets, 200mg, 2 tablets per pack, that were recalled by Generic Pharmaceutical Services, Inc. due to failing USP limit for impurity during stability testing. Failure at this level does not constitute a health hazard per the manufacturer, Interpharm, Inc.
Please check your inventory for the above products 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.
December 28, 2007
Recall Flash – Retail Level Recall
Product: First Aid Kit(AMA Approved)FAO4
Moore's Re-order#: 83323
Lot #: I0247, I0217, I0127, H0307, D0177, D0167, D0027
Manufacturer: First Aid Only
PRODUCT SUBJECT TO RECALL
First Aid Only, Inc. is conducting a voluntary recall of First Aid Only branded first aid kits and/or refills with the lot numbers listed above. These first aid kits and/or refills contain ibuprofen tablets, 200mg, 2 tablets per pack, that were recalled by Generic Pharmaceutical Services, Inc. due to failing USP limit for impurity during stability testing. Failure at this level does not constitute a health hazard per the manufacturer, Interpharm, Inc.
Please check your inventory for the above products 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.
November 29, 2007
Recall Flash – Retail Level Recall
Product: Robitussin Cough DM, Robitussin Chest Congestion
Moore's Re-order#: 02100, 02102
Lot #:All
Manufacturer: Wyeth Consumer Healthcare
PRODUCT SUBJECT TO RECALL
Wyeth Consumer Healthcare is voluntarily recalling these products from the market as these products do not contain a dosing cup with a 1/2 teaspoon mark and the dosing instructions on the labeling include a 1/2 teaspoon every 4 hours for children 2 years to under 6 years.
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.
September 17, 2007
Recall Flash – Retail Level Recall
Product:Atropine Sulfate 0.1mg/ml PSSG
Atropine Sulfate 0.1mg/ml PFS
Moore's Re-order#: 72763 67019
Lot #:
AS031G5 and AS032G5
AS033H5 and AS036J5
Manufacturer: IMS
PRODUCT SUBJECT TO RECALL
International Medication Systems, Ltd. is recalling the above mentioned products with the lot numbers listed above due to failure to maintain full potency through the labeled expiration dates. Use of this product could result in possible health hazard.
Please check your inventory for the above products 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.
August 23, 2007
Recall Flash – Retail Level Recall
Product:Saline Flush Syringe 10mL
Moore's Re-order#: 82915
Lot #:070523SFR, 070620SFR
Manufacturer:B Braun
PRODUCT SUBJECT TO RECALL
B Braun is initiating a product removal of the above products and lot numbers, due to various reports regarding particulate matter in finished good catalog number 513587.
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.
August 23, 2007
Recall Flash – Retail Level Recall
Product:Sodium Chloride 0.9% 10mL
Prefilled Syringe
Moore's Re-order#: 83882
Lot #:070523SFR, 070620SFR
Manufacturer:B Braun
PRODUCT SUBJECT TO RECALL
B Braun is initiating a product removal of the above products and lot numbers, due to various reports regarding particulate matter in finished good catalog number 513587.
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.
July 23, 2007
Recall Flash – Retail Level Recall
Product:Lidocaine Hydrochloride Injection 1% USP
Moore's Re-order#: 79022
Lot #:39-467-DK, 41-243-DK
Manufacturer:Hospira
PRODUCT SUBJECT TO RECALL
Hospira initiated a voluntary recall of two lots of Lidocaine due to reports of particulate in some of the vials. The particulate has been identified as a rubber compound from equipment used in the manufacturing process.
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.
06/08/2007
Recall Flash – Retail Level Recall
Product:Lidocaine Hydrochloride Injection 1% USP
Moore's Re-order#: 79022
Lot #:36-410-DK, 37-478-DK, 39-468-DK, 39-272-DK, 41-242-DK, 42-167-DK, 45-430-DK, 40-380-DK, 40-471-R1
Manufacturer:Hospira
PRODUCT SUBJECT TO RECALL
We have been notified by Hospira of a Retail Level recall on the following product.
Hospira initiated a voluntary recall of two lots of Lidocaine previously due to reports of particulate in some of the vials. They conducted an expanded investigation and as a precaution are recalling additional lots (above) where the issue affecting the initial lots may have potentially existed during the manufacture of the lots listed above.
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.
06/08/2007
Flash – Retail Level Recall
Product:ThyroTest
Moore's Re-order#: 78229
Lot #:21086-02
Manufacturer:Inverness Medical
PRODUCT SUBJECT TO RECALL
We have been notified by Inverness Medical of a Retail Level recall on the following product.
Inverness Medical is voluntarily recalling the above product and lot number due to routine surveillance testing the external positive control supplied within the kit may not produce a signal within the 10 minute test time.
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.
06/08/2007
Recall Flash – Retail Level Recall
Product:Spray & Stretch Fine Stream 3.5oz, Pain Ease Mist Spray 3.5oz, Pain Ease Med Stream Spray 3.5oz
Moore's Re-order#: 75469
Lot #:8019, 8020, 8021, 8022, 4256, 4257, 4258, 6257, 6258, 6259, 6260, 6261
77179, 77178
Manufacturer:Gebauer Company
PRODUCT SUBJECT TO RECALL
We have been notified by Gebauer Company of a Retail Level recall on the following products.
Gebauer Company is proactively and conservatively recalling the above products and lot numbers listed above because they may contain some units that do not meet Gebauer’s internal specification for mold and yeast per USP <61> Microbial Limits. The problem was discovered during their internal investigation into possible cross contamination from another Gebauer product.
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.
06/08/2007
Recall Flash – Retail Level Recall
Product:GreenLine®/D™ Disposable Stainless Mac Laryngoscope Blade
Moore's Re-order#: 80669
Lot #:Gj, Ha, Hc
Manufacturer:SunMed
PRODUCT SUBJECT TO RECALL
We have been notified by SunMed of a Retail Level recall on the following product.
SunMed is recalling the above product and lot numbers based on a concern of a possible defect of the clear, acrylic light bundle. There is a potential for the bundle to break during use.
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.
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