Impurities/Degradation Products: High Out of Specification levels for carbostyril, a known degradation product of diazepam.
Impurities/Degradation Products: High Out of Specification levels for carbostyril, a known degradation product of diazepam.
We break every recall down into plain English — this one’s still on our list. Until our write-up is ready, the official FDA hazard and remedy below have the full, accurate details.
We’ve drafted a message you can send Meridian Medical Technologies a Pfizer Company to request your refund or repair — edit it as you like.
Subject: Recall D-1369-2012 — Meridian Medical Technologies a Pfizer Company Meridian Medical Technologies a Pfizer Company recal Hello, I own a Meridian Medical Technologies a Pfizer Company recalls Diazepam Injection, USP, 10 mg Automatic, Autoinjector for Buddy Use, 5 mg/mL, 2 mL autoinjector, 15-count that is covered by recall D-1369-2012 from Meridian Medical Technologies a Pfizer Company. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
