FlaggedRx← Medication recall checkHome
Class II · ModerateRecall completed

Lisinopril 10 mg tablets

Could cause temporary or reversible harm; serious harm is unlikely.

Does this affect you?
Check your lot numberLot # J0636336-073022, J0637605-080422, Exp. date 08/31/2023
Where it was soldDistributed to two direct accounts in PA and AK.
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

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

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Distributed by / forRemedyRepack Inc.
NDC68180-0980-03
Show the full FDA record
Full product labelLisinopril 10 mg tablets, 30-count Blister Card, Rx Only, MFG: Lupin Pharma, Baltimore, MD Repackaged by: RemedyRepack Inc, Indiana PA. Original NDC# 68180-0980-03, Repackaged NDC# 70518-0468-00
Recalling firmRemedyRepack Inc.
DistributionDistributed to two direct accounts in PA and AK.
Quantity1,699 blister cards/30 tablets each
Recall initiated2022-09-15
Report date2022-09-21
Recall completed2022-11-16
Recall numberD-1538-2022
ClassificationClass II
FDA statusTerminated
Origin on fileIndiana PA United States

Related

Lisinopril recallsRecent drug recallsCheck another medication

Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.