D-1250-2020 Class II Terminated

Recalled by Lupin Pharmaceuticals Inc. — Baltimore, MD

Recall Details

Product Type
Drugs
Report Date
April 29, 2020
Initiation Date
April 20, 2020
Termination Date
June 7, 2021
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
11,808 bottles

Product Description

Lisinopril Tablets USP, 20 mg, 1000-count bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore MD 21202, Manufactured by: Lupin Limited Pithampur (M.P.) 454 775, India. NDC 68180-0981-03

Reason for Recall

Product Mix-Up: a complaint received indicating mix-up of 10 mg Lisinopril tablets inside of 2 sealed bottles of 20 mg/1000 count bottles.

Distribution Pattern

Product was distributed Nationwide in the United States.

Code Information

Lot # Q000255, Exp 01/2022