Lisinopril Tablets USP, 30 mg, 100-count bottle, Rx only, Manufactured for: Lupin Pharmaceuticals...

FDA Recall #D-1079-2020 — Class II — April 1, 2020

Recall #D-1079-2020 Date: April 1, 2020 Classification: Class II Status: Terminated

Product Description

Lisinopril Tablets USP, 30 mg, 100-count bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, Maryland 21202, NDC 68180-982-01

Reason for Recall

Presence of Foreign Tablet/ Capsule: Product complaint received indicating mix-up of one lisinopril 5mg tablet inside of a 30 mg, 100-count bottle of Lisinopril Tablets.

Recalling Firm

Lupin Pharmaceuticals Inc. — Baltimore, MD

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Drugs

Product Quantity

25,944 bottles

Distribution

U.S.A. Nationwide

Code Information

Lot #: Q900580, Exp 9/2021

Status

Terminated

Voluntary / Mandated

Voluntary: Firm initiated