Pfizer recalls Accuretic 20mg/25mg tablets due to impurities exceeding safe levels. Affected lots made in Germany, expiring Feb 2023. Consumers should check NDC 0071-0223-23 and lot number ET6974.
CGMP Deviations: N-nitroso-quinapril and N-nitroso-hydrochlorothiazide impurity above the acceptable daily intake limit.
Pfizer is recalling Accuretic (quinapril HCl/hydrochlorothiazide) tablets that contain impurities potentially exceeding safe levels. This recall affects specific lots made in Germany with expiration date February 2023. The impurities could pose a health risk if taken regularly.
The tablets contain N-nitroso-quinapril and N-nitroso-hydrochlorothiazide impurities that may exceed the acceptable daily intake limit. These impurities could potentially cause health issues if taken regularly over time.
Prescription holders of Accuretic 20mg/25mg tablets with NDC 0071-0223-23 and lot number ET6974. Patients on this medication who have been prescribed by a doctor are most at risk.
Check for NDC code 0071-0223-23 and lot number ET6974 on the bottle. The tablets were made in Germany and expire February 2023.
Look for NDC 0071-0223-23 and lot number ET6974 on the bottle label.
Pfizer recalls these tablets due to impurities (N-nitroso-quinapril and N-nitroso-hydrochlorothiazide) that may exceed safe levels.
Check the NDC code and lot number on the bottle. If it matches 0071-0223-23 and ET6974, contact your doctor or pharmacist.
The recall indicates potential impurities exceeding safe levels, so it's recommended to check if you have the affected lot before using.
We’ve drafted a message you can send Pfizer to request your refund or repair — edit it as you like.
Subject: Recall D-0757-2022 — Pfizer Pfizer Hello, I own a Pfizer that is covered by recall D-0757-2022 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.
