Hospira Inc. recalls Heparin Sodium in 5% Dextrose Injection, Heparin, 25,000 USP Heparin Units/250 mL (100 USP Heparin Units/mL), 250 mL, Si
Recalled July 16, 2014 · FDA recall D-1425-2014 · Hospira
Hazard
Lack of Assurance of Sterility: Confirmed consumer report of fluid leaking from primary container of bag. · FDA Class II
Units
142,152 bags
Sold at
Nationwide
Description
Lack of Assurance of Sterility: Confirmed consumer report of fluid leaking from primary container of bag.
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
Manufacturer(s)
Hospira Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →