Hospira, Inc. recalls Furosemide Injection USP (10 mg/mL), 4 mL in 5 mL Fliptop Vial, Rx only, Hospira Inc., Lake Forest, IL --- NDC 0409-6102
Recalled March 6, 2013 · FDA recall D-169-2013 · Hospira
Hazard
Lack of Assurance of Sterility; possible loose crimp applied to fliptop vial · FDA Class II
Units
63,900 vials
Sold at
Nationwide
Description
Lack of Assurance of Sterility; possible loose crimp applied to fliptop vial
Product
Furosemide Injection USP (10 mg/mL), 4 mL in 5 mL Fliptop Vial, Rx only, Hospira Inc., Lake Forest, IL --- NDC 0409-6102-04
Manufacturer(s)
Hospira, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →