drugs Class II Updated 2014-01-08

Teva Pharmaceuticals USA recalls Daunorubicin Hydrochloride Injection, 20 mg/4 mL (5 mg/mL),

Recalled 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)

Hazard / Issue

Presence of Precipitate; precipitation of drug product

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Lot number EXP 31314801B, 2/2014; 31314990B, 2/2014; 31314991B, 2/2014; 31315014B, 2/2014; 31315155B, 6/2014; 31315279B, 6/2014; 31315837B, 10/2014; 31315921B, 10/2014; 31316029D, 12/2014; and 31316029C, 12/2014
View official government recall

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