RecallRadar

FDA Drug recall D-1413-2020

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

On 2020-08-05 the FDA classified a Class II recall of Lisinopril Tablets USP, 10 mg, 1000 count bottles, Manufactured by: Lupin Limited, Nagpur INDIA, For BluePoint Laboratories NDC 68001-334-08 by Lupin Pharmaceuticals, citing presence of Foreign Tablets/Capsules: Lisinopril Tablets USP, 20mg found in a 1000 count bottle of Lisinopril Tablets USP, 10mg.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1413-2020
ClassificationClass II
Statusterminated
Initiated2020-07-17
Published2020-08-05
Last updated2026-09-13 11:52 UTC
CompanyLupin Pharmaceuticals
DistributionUS

Product

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

Reason

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

Identifiers

ndc68001-337-00
ndc68001-337-08
ndc68001-332-00
ndc68001-332-03
ndc68001-333-00
ndc68001-333-08
ndc68001-486-00
ndc68001-486-08
ndc68001-334-00
ndc68001-334-08
ndc68001-335-00
ndc68001-335-08
ndc68001-336-00
code_infoLot # Q000232, exp. date 01/2022

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1413-2020%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.