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.
Class I - DangerousWhat Should You Do?
- Check if you have this product: Lot #: 8D1082, Exp 01/13; 8D1151, Exp 03/13
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Meridian Medical Technologies a Pfizer Company
- Reason for Recall:
- Impurities/Degradation Products: High Out of Specification levels for carbostyril, a known degradation product of diazepam.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
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.
Product Codes/Lot Numbers:
Lot #: 8D1082, Exp 01/13; 8D1151, Exp 03/13
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: D-1369-2012
Related Recalls
Defective Delivery System; reports of the device failing to activate which could result in a patient not receiving medication
Defective Delivery System; reports of the device failing to activate which could result in a patient not receiving medication