Pfizer recalls 20mg/25mg quinapril and hydrochlorothiazide tablets due to potential impurities that could exceed safe levels. This is a prescription-only product distributed by Greenstone LLC.
CGMP Deviations: N-nitroso-quinapril and N-nitroso-hydrochlorothiazide impurity above the acceptable daily intake limit.
Pfizer is recalling prescription quinapril and hydrochlorothiazide tablets that may contain impurities exceeding safe limits. This could pose a health risk if taken regularly over time.
The tablets may contain N-nitroso-quinapril and N-nitroso-hydrochlorothiazide impurities in amounts above the acceptable daily intake limit. These impurities could potentially cause health issues with long-term use, though the risk is not immediate.
Prescription patients who have the specific 20mg/25mg tablets with NDC 59762-5225-9 and lot FE3714. People taking blood pressure medication who have this exact product are most at risk.
Check for the specific 20mg/25mg quinapril and hydrochlorothiazide tablets in 90-count bottles with NDC 59762-5225-9 and lot number FE3714. These were distributed by Greenstone LLC in the US.
Look for the specific 20mg/25mg quinapril and hydrochlorothiazide tablets with NDC 59762-5225-9 and lot FE3714.
The recall is due to potential impurities that could exceed safe levels with long-term use, but the product is not immediately dangerous.
Check for the specific 20mg/25mg quinapril and hydrochlorothiazide tablets with NDC 59762-5225-9 and lot FE3714.
The recall does not specify a remedy, so contact your doctor or pharmacist for advice.
We’ve drafted a message you can send Pfizer to request your refund or repair — edit it as you like.
Subject: Recall D-0758-2022 — Pfizer Pfizer Hello, I own a Pfizer that is covered by recall D-0758-2022 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.
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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.
