Drug recall D-313-2013

Class II Terminated reported May 15, 2013

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

Reason for recall

Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.

Lots and codes

Lot 05-585-EV Exp. 05/13

Recall details

Recalling firm
Hospira Inc., Lake Forest, IL
Quantity
114,000 vials
Distribution
Nationwide and Puerto Rico
Type
Voluntary: Firm initiated
Recall initiated
February 26, 2013
Terminated
November 10, 2014

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