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sanofi-aventis US Recalls
3 recalls on record · July 11, 2012 to January 2, 2013 · Drugs, Medical Devices
Recalls by year
12
13
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
Also filed under
The recall feeds record what looks like the same company under more than one name:
January 2, 2013Medical DevicesFDA
sanofi-aventis US, Inc. recalls Diamigo i-Phone App The Diamigo app was intended for use as an educational tool in the management of diabetes.
Hazard: Diamigo, a software application, was released through the i-Phone Global Store which inadvertently allowed global access to the application as opposed to the original intended restriction of access to Brazil.
July 11, 2012DrugsFDA
sanofi-aventis US, Inc. recalls Eloxatin (OXALIplatin injection) 5 mg/mL injection, 100 mg, Rx only, Mfd. for: sanofi aventis US LLC Bridgewater, NJ 08
Hazard: CGMP Deviations: Eloxatin was manufactured by Ben Venue Laboratories, a contract manufacturer, which was recently inspected by the agency and revealed significant issues in Good Manufacturing Practices.
July 11, 2012DrugsFDA
sanofi-aventis US, Inc. recalls Eloxatin (OXALIplatin injection) 5 mg/mL Injection, 50 mg, Rx only, Mfd. for: sanofi aventis US LLC Bridgewater, NJ 0880
Hazard: CGMP Deviations: Eloxatin was manufactured by Ben Venue Laboratories, a contract manufacturer, which was recently inspected by the agency and revealed significant issues in Good Manufacturing Practices.