Quinapril: 5 recalls on record
Recalled by 1 agency: FDA (5).
First recall on record: January 22, 2014. Most recent: December 28, 2022.
Risk classification: Class II: 4 · Class III: 1
Most recent recalls
| Date | Agency | Product | Recall number |
|---|---|---|---|
| December 28, 2022 | FDA | Quinapril Tablets USP, 40 mg (90 pack), Rx Only, Manufactured for: Lupin Pharmaceuticals,…D-0088-2023 | D-0088-2023 |
| December 28, 2022 | FDA | Quinapril Tablets USP, 20 mg (90 pack), Rx Only, Manufactured for: Lupin Pharmaceuticals,…D-0089-2023 | D-0089-2023 |
| April 12, 2017 | FDA | Quinapril Tablets USP 5 mg, 90 count bottles, Lupin Pharmaceuticals, Inc., Baltimore, MD …D-0650-2017 | D-0650-2017 |
| January 22, 2014 | FDA | Quinapril Tablets USP, 10 mg, 90 count bottle, Rx only, Manufactured for: Lupin Pharmace…D-409-2014 | D-409-2014 |
| January 22, 2014 | FDA | Quinapril Tablets USP, 5 mg, 90 count bottle, Rx only, Manufactured for: Lupin Pharmaceu…D-408-2014 | D-408-2014 |
Questions about this brand
- How many recalls does Quinapril have?
- Recalert has 5 U.S. recalls on record for Quinapril, published between January 22, 2014 and December 28, 2022.
- What was the most recent Quinapril recall?
- FDA recall D-0088-2023, published December 28, 2022: Quinapril Tablets USP, 40 mg (90 pack), Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202, by: Lupin Limited, Goa 403 722 India, NDC# 68180-554-09
- Which agencies have recalled Quinapril products?
- Quinapril products appear in recalls from: FDA (5).
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