FDAFDA · Food and drugs·Recall number D-1369-2012
Diazepam Injection, USP, 10 mg Automatic, Autoinjector for Buddy Use, 5 mg/mL, 2 mL autoinjector, 15-count autoinjectors per carton, Rx only, Meridian Medical Technologies, Columbia, MD 21046; A subsidiary of King Pharmaceuticals, Inc.; NSN 6505-01-274-0951, NDC 11704-600-01.
Published June 20, 2012 · Recall initiated: June 6, 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
Impurities/Degradation Products: High Out of Specification levels for carbostyril, a known degradation product of diazepam.
What to do
Voluntary: Firm initiated · Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Recall details
- Brand
- DIAZEPAM
- Manufacturer
- Meridian Medical Technologies a Pfizer Company
- Distributor
- Nationwide, military, Italy, Singapore, Sweden, and Canada.
- UPC
- 0311704600015
- Lot
- Lot #: 8D1082, Exp 01/13; 8D1151, Exp 03/13
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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