Data Foundry

Drug recalls 2020

Lisinopril Tablets USP — Class II drug recall D-1413-2020

Terminated recall by Lupin Pharmaceuticals Inc., reported 2020-08-05, distributed nationwide. Presence of Foreign Tablets/Capsules: Lisinopril Tablets USP, 20mg found in a 1000 count bottle of Lisinopril

Recall numberD-1413-2020
Product typeDrug
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmLupin Pharmaceuticals Inc., Baltimore, MD, United States
Recall initiated2020-07-17
Classified2020-07-28
Reported by FDA2020-08-05
Terminated2021-08-26
DistributedNationwide (US)
Quantity11,688 bottles
NDC68001-0332, 68001-0332-00, 68001-0332-03, 68001-0333, 68001-0333-00, 68001-0333-08, 68001-0334, 68001-0334-00, 68001-0334-08, 68001-0335, 68001-0335-00, 68001-0335-08, 68001-0336, 68001-0336-00, 68001-0337, 68001-0337-00, 68001-0337-08, 68001-0486, 68001-0486-00, 68001-0486-08
Lot numbersQ000232
Expiration dates2022-01

Product

Lisinopril Tablets USP, 10 mg, 1000 count bottles, Manufactured by: Lupin Limited, Nagpur INDIA, For BluePoint Laboratories NDC 68001-334-08

Reason for recall

Presence of Foreign Tablets/Capsules: Lisinopril Tablets USP, 20mg found in a 1000 count bottle of Lisinopril Tablets USP, 10mg

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-1413-2020. 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.