Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Accupril (Quinapril HCl Tablets) 40 mg Recalled by Pfizer Inc. Due to CGMP Deviations: Contains N-nitrosoquinapril above the acceptable limits.
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Pfizer Inc. directly.
Affected Products
Accupril (Quinapril HCl Tablets) 40 mg, 90 Tablets, Rx only NDC 0071-0535-23 Distributed by: Parke-Davis Division of Pfizer Inc. NY, NY 10017
Quantity: 8346 bottles
Why Was This Recalled?
CGMP Deviations: Contains N-nitrosoquinapril above the acceptable limits.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Pfizer Inc.
Pfizer Inc. has 114 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report