FDAFDA · Food and drugs·Recall number D-309-2013
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
Published May 8, 2013 · Recall initiated: August 28, 2012
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- DIAZEPAM
- Manufacturer
- Hospira Inc.
- Distributor
- Nationwide and Puerto Rico
- Lot
- Lot 17-100-EV and 17-399-EV
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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