Teva Pharmaceuticals USA, Inc. recalls CARBOplatin Injection, 600 mg/60ml, MultiDose, Rx only, Teva Parenteral Medicines, Inc., Irvine, CA 92618 NDC 0703-3249-
Recalled September 11, 2013 · FDA recall D-928-2013 · Teva Pharmaceuticals USA
Hazard
Lack of Assurance of Sterility: The required reduction of endotoxin was not met during the annual revalidation of the vial washer. · FDA Class II
Units
780 vials
Sold at
Nationwide
Description
Lack of Assurance of Sterility: The required reduction of endotoxin was not met during the annual revalidation of the vial washer.
Product
CARBOplatin Injection, 600 mg/60ml, MultiDose, Rx only, Teva Parenteral Medicines, Inc., Irvine, CA 92618 NDC 0703-3249-11
Manufacturer(s)
Teva Pharmaceuticals USA, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →