Data Foundry

Drug recalls 2022

Lisinopril Tablets USP — Class II drug recall D-1536-2022

Terminated recall by Lupin Pharmaceuticals Inc., reported 2022-09-21, distributed nationwide. Presence of Foreign Substance: Foreign material (metal piece) embedded in one tablet.

Recall numberD-1536-2022
Product typeDrug
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmLupin Pharmaceuticals Inc., Baltimore, MD, United States
Recall initiated2022-09-13
Classified2022-09-15
Reported by FDA2022-09-21
Terminated2024-01-31
DistributedNationwide (US)
Reason classesforeign material
NDC68180-0512, 68180-0512-01, 68180-0512-02, 68180-0512-03, 68180-0512-09, 68180-0512-30, 68180-0513, 68180-0513-01, 68180-0513-02, 68180-0513-03, 68180-0513-05, 68180-0513-09, 68180-0513-30, 68180-0514, 68180-0514-01, 68180-0514-02, 68180-0514-03, 68180-0514-05, 68180-0514-09, 68180-0514-30, 68180-0515, 68180-0515-01, 68180-0515-02, 68180-0515-03, 68180-0515-05 and 40 more
Lot numbersQ201182
Expiration dates2024-03-20

Product

Lisinopril Tablets USP, 10 mg, 1000-count bottles, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202, Manufactured by: Lupin Limited, Nagpur- 441 108, India. NDC 68180-980-03

Reason for recall

Presence of Foreign Substance: Foreign material (metal piece) embedded in one tablet.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1536-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.