Drug recall D-501-2013
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
17-099-EV Exp 05/14
Recall details
- Recalling firm
- Hospira Inc., Lake Forest, IL
- Quantity
- 95,700 vials
- Distribution
- Nationwide and Puerto Rico
- Type
- Voluntary: Firm initiated
- Recall initiated
- May 16, 2013
- Terminated
- November 10, 2014
Related products
- Diazepam – drug information
- NDC 0409-3213 Diazepam · Diazepam 5 mg/mL · Hospira, Inc.