Reported Jun 20, 2012 · Terminated
Diazepam Injection, USP, 10 mg Automatic, Autoinjector for Buddy Use, 5 mg/mL, 2 mL autoinjector, 15-count…
Meridian Medical Technologies a Pfizer Company
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Meridian Medical Technologies a Pfizer Company · 1945 Craig Rd · Saint Louis, MO · 63146-4105
Is this the product you have?
- 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.
- Lot codes and dates
Lot #: 8D1082Exp 01/138D1151Exp 03/13
- Amount recalled
- 83,400 autoinjectors
Where it was sold
- Nationwide
Why it was recalled
Impurities/Degradation Products: High Out of Specification levels for carbostyril, a known degradation product of diazepam.
This product could cause temporary or reversible health problems — stop using it.
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