Hospira Inc. recalls DOBUTamine in 5% Dextrose Injection, USP, 250 mg Total, 1000 mcg/mL 250 mL bag, Rx only, HOPIRA, INC., LAKE FOREST, IL 6
Recalled June 12, 2013 · FDA recall D-502-2013 · Hospira
Hazard
Lack of Assurance of Sterility: Confirmed report of leaking in the primary container. · FDA Class II
Units
44,748 bags
Sold at
Nationwide and Puerto Rico
Description
Lack of Assurance of Sterility: Confirmed report of leaking in the primary container.
Product
DOBUTamine in 5% Dextrose Injection, USP, 250 mg Total, 1000 mcg/mL 250 mL bag, Rx only, HOPIRA, INC., LAKE FOREST, IL 60045 NDC 0409-2346-32
Manufacturer(s)
Hospira Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →