Hospira Inc. recalls Diazepam Injection, USP 5 mg/mL, 10 mL, Multiple-dose flipto
Recalled 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
Hazard / Issue
Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Lot 17-100-EV and 17-399-EV
View official government recall
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