FDA recall record

Lisinopril Tablets, USP, 5 mg recall — FDA D-1290-2020

Product Mix Up: Lisinopril 10 mg tablets were found in Lisinopril 5 mg 1000-count bottle.

Class IIclassification
D-1290-2020official record ID
Jun 17, 2020report date

Recall record at a glance

Official recordD-1290-2020
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmLupin Pharmaceuticals Inc.
Report dateJun 17, 2020
Recall initiation dateMay 28, 2020
Quantity4,224 bottles
LocationBaltimore, MD, United States

Official product description

Lisinopril Tablets, USP, 5 mg, Rx Only, 1000-count bottle, Manufactured for: Lupin Pharmaceuticals Inc., Baltimore, MD 21202, Manufactured by: Lupin Limited, Nagpur - 441 108, India, NDC 68180-513-03.

Why the product was recalled

Product Mix Up: Lisinopril 10 mg tablets were found in Lisinopril 5 mg 1000-count bottle.

Distribution information

Nationwide within the US.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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