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
Reported: May 25, 2022 Initiated: April 22, 2022 #D-0873-2022
Product Description
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
Reason for Recall
CGMP Deviations: Contains N-nitrosoquinapril above the acceptable limits.
Details
- Recalling Firm
- Pfizer Inc.
- Units Affected
- 10,304 bottles
- Distribution
- Nationwide and Puerto Rico
- Location
- New York, NY
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by Pfizer Inc.. Units affected: 10,304 bottles.
Why was this product recalled? ▼
CGMP Deviations: Contains N-nitrosoquinapril above the acceptable limits.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on May 25, 2022. Severity: Moderate. Recall number: D-0873-2022.
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