drugs Class II Updated 2014-07-16

Hospira Inc. recalls Heparin Sodium in 5% Dextrose Injection, Heparin, 25,000 USP

Recalled Product

Heparin Sodium in 5% Dextrose Injection, Heparin, 25,000 USP Heparin Units/250 mL (100 USP Heparin Units/mL), 250 mL, Single-Dose Container, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-7793-62

Hazard / Issue

Lack of Assurance of Sterility: Confirmed consumer report of fluid leaking from primary container of bag.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Lot # 34-811-KL, 36-106-KL, 36-114-KL; Exp. 12/15; 36-101-KL, Exp. 12/15; 37-202-KL, Exp. 1/16; 38-302-KL, Exp. 2/16; 38-305-KL, Exp. 2/16
View official government recall

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