RecallDepth
Class II Terminated

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.

Company
Meridian Medical Technologies A Pfizer Company
Recall Initiated
June 6, 2012
Posted
June 20, 2012
Recall Number
D-1369-2012
Voluntary / Mandated
Voluntary: Firm initiated
Quantity
83,400 autoinjectors
Firm Location
Saint Louis, MO, United States

Reason for Recall

Impurities/Degradation Products: High Out of Specification levels for carbostyril, a known degradation product of diazepam.

Distribution

Nationwide, military, Italy, Singapore, Sweden, and Canada.

Lot / Code Info

Lot #: 8D1082, Exp 01/13; 8D1151, Exp 03/13

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