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
Class I - DangerousWhat Should You Do?
- Check if you have this product: Lots: DX6031 Exp. MAR 31 2023; CK6260 Exp. MAY 31 2022
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Pfizer Inc.
- Reason for Recall:
- CGMP Deviations: Contains N-nitrosoquinapril above the acceptable limits.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
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
Product Codes/Lot Numbers:
Lots: DX6031 Exp. MAR 31 2023; CK6260 Exp. MAY 31 2022
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: D-0874-2022
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