Pfizer Inc. recalls Accupril (Quinapril HCl Tablets) 20 mg, 90 Tablets, Rx only
See all recalls from Pfizer Inc. →Recalled Product
Accupril (Quinapril HCl Tablets) 20 mg, 90 Tablets, Rx only NDC 0071-0532-23 Distributed by: Parke-Davis Division of Pfizer Inc. NY, NY 10017
Hazard / Issue
CGMP Deviations: Contains N-nitrosoquinapril above the acceptable limits.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Lots: DX8682 Exp. MAR 31 2023; DG1188 Exp. MAR 31 2022
✅ What Should You Do?
- 1Stop taking this medication and contact your doctor or pharmacist immediately.
- 2Do NOT flush medications down the drain — use an FDA-approved drug take-back program.
- 3Check the lot number on your bottle or packaging against the recalled lots listed above.
- 4Report adverse events to FDA MedWatch or call 1-800-FDA-1088.
Looking for a safe alternative?
Search Amazon for Accupril (Quinapril HCl Tablets) →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
Get the next US recall alert before it hits the news.
Free. Weekly digest or instant alerts. Unsubscribe anytime.
CAN-SPAM compliant · No spam · Unsubscribe anytime