Defibtech, LLC, is
initiating a voluntary recall of 5,418 DBP-2800 Battery Packs used in the Lifeline AED®
and ReviveR AEDTM (semi-automatic external defibrillators). This recall affects all DBP-
2800 Battery Packs shipped prior to June 4, 2007. In rare instances, when the AED is
used with an affected battery pack, the AED may falsely detect an error condition during
charging for a shock, then cancel charge and not provide therapy. Defibtech determined
the need for this recall after learning of four reports from end users of this malfunction
during patient use.
West-Ward Pharmaceuticals Recalls Ondansetron in 5% Dextrose Injection And Metronidazole Injection, USP Bags Due To Possible Health Risk
West-Ward Pharmaceuticals Inc., of Eatontown, NJ, is voluntarily recalling all lots of Claris LifeSciences Inc. manufactured Ondansetron in 5% Dextrose Injection, supplied in 32mg/50mL Single-Use Plastic Bag Containers and Metronidazole Injection 500mg/100ml USP in Flexible IV Plastic Bag Containers. Claris recently received reports of the presence of floating matter and non-sterility in Ondansetron and Metronidazole. Non-sterile products administered intravenously may cause infections which could be fatal especially in patients who are immuno-compromised.
Pfizer Initiates a Nationwide Voluntary Recall of All Lots of Metronidazole Injection, Ciprofloxacin Injection, and Ondansetron Injection Bags Made by Claris Lifesciences Due to Non-Sterility
Pfizer Inc is voluntarily recalling Metronidazole, Ciprofloxacin and Ondansetron IV Products due to the presence of floating matter and non-sterility discovered by the manufacturer Claris Laboratories. Non-sterility of a product administered via the intravenous route has the potential to result in infections, which could be fatal, especially in patients who are immunocompromised. Metronidazole and Ciprofloxacin injections are intravenous antibiotics used to treat infections.
Sagent Pharmaceuticals Initiates a Nationwide Voluntary Recall of All Lots of Ondansetron in 5% Dextrose Injection, 32 mg/50 mL Manufactured by Claris Lifesciences
Sagent Pharmaceuticals, Inc. today announced the voluntary nationwide recall of all lots of ondansetron injection in 5% dextrose 32mg / 50 mL (NDC number 25021-776-50) manufactured by Claris Lifesciences and distributed by Sagent. The lot numbers being recalled are: A090309, A090310, A090311 and A090312, which were distributed to hospitals, wholesalers and distributors nationwide from August 2009 through May 2010. Ondansetron injection is an intravenous product used to treat nausea and vomiting associated with chemotherapy or surgery and is supplied in a single dose plastic container.
Eastern Fish Recalls Hannaford and Bloom Private Brand Frozen Raw Extra Jumbo Shrimp Packaged in 16 oz. Bags, Product of Mexico
Eastern Fish is alerting consumers that Hannaford Supermarkets and Bloom brands of frozen raw extra jumbo (16/20) shrimp in 16 oz packages, as well as these brands of shrimp from the full-service seafood cases, labeled as product of Mexico, sold May 4 through June 4 at Hannaford Supermarkets and sold April 8 through June 4 at Bloom grocery stores, are subject to a voluntary recall because the products may contain undeclared sulfites. People who have an allergy or sensitivity to sulfites risk an allergic reaction if they consume these products.
Kent Nutrition Group, Inc. Undertakes Limited Recall of Kent Feeds 20 Lamb DQ45 Medicated
Kent Nutrition Group, Inc. is voluntarily recalling 36 bags of one specific lot of its Kent Feeds 20 Lamb DQ45 Medicated. The recall is being implemented due to the discovery of excess amounts of copper in the feed from lot number 810127. At the time the recall was issued, no customer complaints had been received and no animal health issues had been reported.
Claris Lifesciences initiates a nationwide voluntary recall of all lots of Ciprofloxacin Inj. USP 200 mg / 100 mL, Ciprofloxacin Inj. USP 400 mg / 200 mL, Metronidazole Inj. USP 500 mg/100 ml and Ondansetron Inj., 32 mg / 50 mL.
Claris Lifesciences today announces the voluntary nationwide recall of all lots of Ciprofloxacin Inj. USP 200 mg / 100 mL (NDC 36000-008-24), Ciprofloxacin Inj. USP 400 mg / 200 mL (NDC 36000-009-24), Metronidazole Inj. USP 500 mg/100 ml (NDC 36000-001-24), and Ondansetron in 5% Dextrose Inj. 32 mg / 50 mL (36000-014-06) manufactured and distributed by Claris Lifesciences. All lots are being recalled, which were distributed to hospitals, wholesalers and distributors nationwide.
Better Made Snack Foods Issues an Allergy Alert on Undeclared Dairy in the 3-Ounce Better Made Special Original Potato Sticks
Better Made Snack Foods of Detroit, Michigan is issuing a voluntary recall only of their Better Made 3-ounce Original Potato Sticks because it may contain undeclared dairy. People who have allergies to dairy run the risk of an allergic reaction.
Blacksmith Brands Announces Nationwide Voluntary Recall Of Four PediaCare Children’s Products
Blacksmith Brands, Inc., in consultation with the U.S. Food and Drug Administration, is voluntarily recalling all lots of four children’s products in the PediaCare line. These products are sold exclusively in the United States.
Hospira Announces an Expansion of a Nationwide Voluntary Recall of Certain Lots of Liposyn™ and Propofol That May Contain Particulate Matter
Hospira, Inc. (NYSE: HSP), a global specialty pharmaceutical and medication delivery company, announced today it is voluntarily expanding its March 31, 2010, recall of Propofol Injectable Emulsion 1% and Liposyn™ (Intravenous Fat Emulsion) products which include Liposyn II 10%, Liposyn II 20%, Liposyn III 10%, Liposyn III 20%, and Liposyn III 30% to the consumer or user level. Hospira is conducting the recall because some of the containers may contain particulate matter.