Lupin Pharmaceuticals Inc. 2022-12-28 Health serious FDA
Health · FDA · Recall #FDA-D-0089-2023
Quinapril Tablets USP, 20 mg (90 pack), Rx Only, Manufactured for: Lupin Pharmaceuticals,… Recall
Issued December 28, 2022 · Lupin Pharmaceuticals Inc.
In December 2022, Lupin Pharmaceuticals Inc. recalled the Quinapril Tablets USP, 20 mg (90 pack), Rx Only, Manufactured for: Lupin Pharmaceuticals,…, a serious health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.
Compiled by Maya Ellison, RecallCheckr
What this means for you
CGMP Deviations: Detection of N-Nitroso-quinapril impurity above the acceptable daily intake limit.
What you should do
- 1 Stop using Quinapril Tablets USP, 20 mg (90 pack), Rx Only, Manufactured for: Lupin Pharmaceuticals,… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Lupin Pharmaceuticals Inc. to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Lupin Pharmaceuticals Inc.
- Category
- Health
- Recall date
- December 28, 2022
- Units affected
- Not reported
- Sold at
- Product was distributed by major distribution chains nationwide.
- Recall number
- FDA-D-0089-2023
- Made in
- United States
- Issuing agency
- FDA
In context
- Lupin Pharmaceuticals Inc. has 19 recalls in our database, including 1 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 870th Health recall we've logged in 2022.