Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Quinapril Tablets USP 5 mg Recalled by Lupin Pharmaceuticals Inc. Due to Failed Impurities/Degradation Specifications; Impurity A
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 Lupin Pharmaceuticals Inc. directly.
Affected Products
Quinapril Tablets USP 5 mg, 90 count bottles, Lupin Pharmaceuticals, Inc., Baltimore, MD --- NDC 68180-556-09
Quantity: 15,168 bottes
Why Was This Recalled?
Failed Impurities/Degradation Specifications; Impurity A
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Lupin Pharmaceuticals Inc.
Lupin Pharmaceuticals Inc. has 119 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report