Hospira Inc. recalls Furosemide Injection, USP, 40 mg/4mL (10 mg/mL), 4 ml Single-Dose Vial, Rx only, HOSPIRA, INC. LAKE FOREST, IL 60045 USA
Recalled May 15, 2013 · FDA recall D-314-2013 · Hospira
Hazard
Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial. · FDA Class II
Units
259,050 vials
Sold at
Nationwide and Puerto Rico
Description
Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.
Product
Furosemide Injection, USP, 40 mg/4mL (10 mg/mL), 4 ml Single-Dose Vial, Rx only, HOSPIRA, INC. LAKE FOREST, IL 60045 USA, NDC 0409-6102-04
Manufacturer(s)
Hospira Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →