Hospira Inc. recalls Diazepam Injection, USP 5 mg/mL, 10 mL, Multiple-dose fliptop vial, RX only, HOSPIRA, INC. LAKE FOREST, IL 60045 USA, ND
Recalled June 12, 2013 · FDA recall D-501-2013 · Hospira
Hazard
Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial. · FDA Class II
Units
95,700 vials
Sold at
Nationwide and Puerto Rico
Description
Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.
Product
Diazepam Injection, USP 5 mg/mL, 10 mL, Multiple-dose fliptop vial, RX only, HOSPIRA, INC. LAKE FOREST, IL 60045 USA, NDC 0409-3213-12
Manufacturer(s)
Hospira Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →