Pfizer recalls 20 mg/12.5 mg quinapril HCl/hydrochlorothiazide tablets due to impurities that may exceed safe levels. Affected lots manufactured in Germany, expiring March 2023.
CGMP Deviations: N-nitroso-quinapril and N-nitroso-hydrochlorothiazide impurity above the acceptable daily intake limit.
Pfizer is recalling certain quinapril tablets that may contain impurities in amounts exceeding 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 levels above the acceptable daily intake limit. These impurities could potentially cause health issues if taken regularly.
People with prescriptions for these specific tablets. Those who have the 90-tablet bottles labeled with NDC 59762-0220-1 and lots DN6931, ED3904, or ED3905 are most at risk.
Check for the product name 'quinapril HCl/hydrochlorothiazide tablets, 20 mg/12.5 mg', 90 tablets, Rx only. Look for NDC 59762-0220-1 and lots DN6931, ED3904, or ED3905.
Identify the NDC number and lot numbers on the bottle to confirm if it's affected.
The recall is due to potential impurities that may exceed safe levels. Do not take these tablets until you confirm they are not affected.
Check the NDC number and lot numbers on the bottle. If it matches the affected lots, stop using it and contact Pfizer for guidance.
The recall record does not specify a replacement process. Contact Pfizer directly for assistance.
We’ve drafted a message you can send Pfizer to request your refund or repair — edit it as you like.
Subject: Recall D-0759-2022 — Pfizer Pfizer Hello, I own a Pfizer that is covered by recall D-0759-2022 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.
