Teva Pharmaceuticals USA recalls Daunorubicin Hydrochloride Injection, 20 mg/4 mL (5 mg/mL), 4 mL Single Dose Vial, Rx ONLY, For IV Use Only, Manufacture
Recalled January 8, 2014 · FDA recall D-392-2014 · Teva Pharmaceuticals USA
Hazard
Presence of Precipitate; precipitation of drug product · FDA Class II
Units
13520 vials
Sold at
Nationwide
Description
Presence of Precipitate; precipitation of drug product
Product
Daunorubicin Hydrochloride Injection, 20 mg/4 mL (5 mg/mL), 4 mL Single Dose Vial, Rx ONLY, For IV Use Only, Manufactured By: Teva parenteral Medicines, Inc., Irvine, CA NOVAPlus¿¿ labels. NDC 0703-5233-13 (carton), NDC 0703-5233-11 (vial) or NDC 0703-5233-93 (carton), NDC 0703-5233-91 (vial)
Manufacturer(s)
Teva Pharmaceuticals USA
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →