Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Diazepam Injection Recalled by Meridian Medical Technologies a Pfizer Company Due to Impurities/Degradation Products: High Out of Specification levels for...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Meridian Medical Technologies a Pfizer Company directly.
Affected Products
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.
Quantity: 83,400 autoinjectors
Why Was This Recalled?
Impurities/Degradation Products: High Out of Specification levels for carbostyril, a known degradation product of diazepam.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Meridian Medical Technologies a Pfizer Company
Meridian Medical Technologies a Pfizer Company has 3 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report