CLASS II Drug recall · Reported 26 Aug 2015 · FDA Enforcement Report

Lisinopril Tablets USP, 5 mg recalled by Wockhardt Usa

Wockhardt Usa is recalling Lisinopril Tablets USP, 5 mg, distributed nationwide in the US. The recall was initiated on 29 Jul 2015 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot #: DM12700, Exp 09/15
Quantity recalled1704 bottles

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-1346-2015
FDA event ID
71946
Recalling firm
Wockhardt Usa, Parsippany, NJ
Classification
Class II
Status
Terminated
Recall initiated
29 Jul 2015
FDA classified
19 Aug 2015
Reported
26 Aug 2015
Type
Voluntary: Firm initiated
Customers notified by
Letter

Timeline

29 Jul 2015Recall initiated by company
19 Aug 2015Classified by FDA+21 days
26 Aug 2015Published in enforcement report+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

CGMP Deviations: An FDA inspection identified inadequate investigations of past market complaints.

Product as listed by the FDA

Lisinopril Tablets USP, 5 mg, 1000-count bottles, Rx Only, Manufactured by: Wockhardt Limited, Mumbai, India; Distributed by: Wockhardt USA LLC, 20 Waterview Blvd, Parsippany, NJ 07054 USA, UPC 3 64679 92806 6, NDC 64679-928-06.

Where it was distributed

Nationwide

Nationwide

Stores named: Walmart

Questions about this recall

Is Lisinopril Tablets USP, 5 mg recalled?

Yes. Wockhardt Usa recalled Lisinopril Tablets USP, 5 mg on 29 Jul 2015. The recall is Class II and its status is Terminated. Recall number D-1346-2015.

Why was it recalled?

CGMP Deviations: An FDA inspection identified inadequate investigations of past market complaints.

Which lots are affected?

Lot #: DM12700, Exp 09/15

Where was it sold?

Nationwide

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

More recalls from Wockhardt Usa

All 45

Other Lisinopril recalls

All 34