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Class II · ModerateRecall completed

Lisinopril

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

Does this affect you?
Check your lot numberLot # Q900683, Exp. 10/31/2022
Where it was soldNationwide within the US.
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

Product Mix Up: Lisinopril 10 mg tablets were found in Lisinopril 5 mg 1000-count bottle.

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

Made byLupin Limited, Nagpur - 441 108, India foreign manufacturer
Brand nameLISINOPRIL
Generic nameLISINOPRIL
Active ingredient(s)LISINOPRIL
Distributed by / forLupin Pharmaceuticals Inc., Baltimore, MD 21202
NDC68180-513-03
Show the full FDA record
Full product labelLisinopril Tablets, USP, 5 mg, Rx Only, 1000-count bottle, Manufactured for: Lupin Pharmaceuticals Inc., Baltimore, MD 21202, Manufactured by: Lupin Limited, Nagpur - 441 108, India, NDC 68180-513-03.
Recalling firmLupin Pharmaceuticals Inc.
DistributionNationwide within the US.
Quantity4,224 bottles
Recall initiated2020-05-28
Report date2020-06-17
Recall completed2021-05-04
Recall numberD-1290-2020
ClassificationClass II
FDA statusTerminated
Origin on fileBaltimore MD 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.