Pfizer recalls Accupril 40mg tablets (NDC 0071-0535-23) due to N-nitrosoquinapril levels exceeding safety limits. This may pose a risk of serious health effects. Contact Pfizer for details.
CGMP Deviations: Contains N-nitrosoquinapril above the acceptable limits.
Pfizer is recalling Accupril 40mg tablets (90 tablets) that were manufactured with N-nitrosoquinapril levels above acceptable limits. This could potentially cause serious health effects if taken as directed.
The recalled tablets contain N-nitrosoquinapril at levels above the acceptable limits set by regulatory standards. N-nitroso compounds are known to be potential carcinogens, which could increase cancer risk with long-term use.
People with a prescription for Accupril 40mg tablets (NDC 0071-0535-23) from Pfizer. Those who have taken the recalled product may be at risk.
Check your prescription label for Accupril 40mg tablets (90 tablets) with NDC 0071-0535-23. The product was distributed by Parke-Davis Division of Pfizer Inc. and was manufactured in specific lots (DX6031, CK6260).
Verify if you have a prescription for Accupril 40mg tablets (NDC 0071-0535-23) from Pfizer.
The recall states the product contains N-nitrosoquinapril above acceptable limits, which may pose a health risk. Do not take the recalled product.
Check your prescription label for Accupril 40mg tablets (90 tablets) with NDC 0071-0535-23. The product was distributed by Parke-Davis Division of Pfizer Inc. and was manufactured in specific lots (DX6031, CK6260).
The recall does not specify a remedy, so contact Pfizer directly for guidance.
We’ve drafted a message you can send Pfizer to request your refund or repair — edit it as you like.
Subject: Recall D-0874-2022 — Pfizer Pfizer Hello, I own a Pfizer that is covered by recall D-0874-2022 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.
