US Drug Recall Register
Class II · Moderate risk Terminated Initiated Apr 22, 2022 (4 years ago)

Accupril (Quinapril HCl Tablets) 10 mg, 90 Tablets Rx only NDC 0071-0530-23 Distributed…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

CGMP Deviations: Contains N-nitrosoquinapril above the acceptable limits.

What was recalled

Accupril (Quinapril HCl Tablets) 10 mg, 90 Tablets Rx only NDC 0071-0530-23 Distributed by: Parke-Davis Division of Pfizer Inc. NY, NY 10017

Recalling firm
Pfizer Inc.
NDC code
0071-0530-23
Origin
NY, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0872-2022

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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