Pfizer recalls Accure: 10 mg/12.5 mg tablets with potential impurities exceeding safe levels. Consumers with prescription bottles should contact their doctor.
CGMP Deviations: N-nitroso-quinapril and N-nitroso-hydrochlorothiazide impurity above the acceptable daily intake limit.
Pfizer is recalling Accuretic tablets that may contain impurities above safe limits. This could pose a health risk if taken as directed.
The tablets may contain N-nitroso-quinapril and N-nitroso-hydrochlorothiazide impurities in amounts exceeding the acceptable daily intake limit. These impurities could potentially cause health issues if consumed regularly.
Prescription patients using Accuretic tablets with the specific lot number FG5379. Those with the 10 mg/12.5 mg strength and 90-tablet bottles are most at risk.
Check for the lot number FG5379 on the bottle. The product is a 10 mg/12.5 mg tablet bottle with 90 tablets, made in Germany, and expires August 2024.
Since this is a prescription medication, you should speak with your healthcare provider about alternative treatment options.
The recall indicates potential impurities above safe limits, but the product is still prescription-only. Consult your doctor for advice.
You should contact your doctor for guidance on whether to stop using it and alternative treatment options.
Look for the lot number FG5379 on the bottle, which is part of the specific 10 mg/12.5 mg tablets with 90 tablets, made in Germany, and expiring August 2024.
We’ve drafted a message you can send Pfizer to request your refund or repair — edit it as you like.
Subject: Recall D-0754-2022 — Pfizer Pfizer Hello, I own a Pfizer that is covered by recall D-0754-2022 from Pfizer. 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.
