FDAClass IIAugust 22, 2018

Lisinopril Tablets USP recall

Lisinopril Tablets USP, 10mg, 1000-count bottles, Rx only, Manufactured for: Lupin Pharmaceuticals Inc. Baltimore, Maryland 21202, NDC 68180-980-03

Why was Lisinopril Tablets USP recalled?

Presence of Foreign Substance: Product complaint was received of metal contaminant observed in one tablet.

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Lot #: H800414, Exp. 12/2019

Product
Lisinopril Tablets USP, 10mg, 1000-count bottles, Rx only, Manufactured for: Lupin Pharmaceuticals Inc. Baltimore, Maryland 21202, NDC 68180-980-03
Recalling firm
Lupin Pharmaceuticals Inc.
Quantity
11,706 bottles
Distribution
Product was distributed to distributors, mail order pharmacy and supermarkets throughout the United States.
Recall date
August 22, 2018
Classification
Class II
Status
Terminated
Agency
FDA (drug)
Open FDA enforcement record Latest recalls