FDAFDA · Food and drugs·Recall number D-927-2013
Diazepam Injection, USP, 5 mg/mL, 10 mL, Multiple-dose Sterile Non-pyrogenic, Fliptop Vial, C-IV, Rx Only, Hospira, Inc., Lake Forest, IL 60045, USA, NDC 0409-3213-12
Published September 4, 2013 · Recall initiated: August 16, 2013
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: ineffective crimp on fliptop vials that may result in leaking at the neck of the vials.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- DIAZEPAM
- Manufacturer
- Hospira Inc.
- Distributor
- Nationwide and Puerto Rico
- Lot
- Lot: 23-505-EV, Exp. 11/14
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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