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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 #: H800414, Exp. 12/2019
Where it was soldProduct was distributed to distributors, mail order pharmacy and supermarkets throughout the United States.
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: Product complaint was received of metal contaminant observed 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

Made byLupin Pharmaceuticals, Inc.
Brand nameLISINOPRIL
Generic nameLISINOPRIL
Active ingredient(s)LISINOPRIL
Distributed by / forLupin Pharmaceuticals Inc. Baltimore, Maryland 21202
NDC68180-980-03
Show the full FDA record
Full product labelLisinopril Tablets USP, 10mg, 1000-count bottles, Rx only, Manufactured for: Lupin Pharmaceuticals Inc. Baltimore, Maryland 21202, NDC 68180-980-03
Recalling firmLupin Pharmaceuticals Inc.
DistributionProduct was distributed to distributors, mail order pharmacy and supermarkets throughout the United States.
Quantity11,706 bottles
Recall initiated2018-08-13
Report date2018-08-22
Recall completed2019-10-15
Recall numberD-1077-2018
ClassificationClass II
FDA statusTerminated
Origin on fileBaltimore MD United States

Related

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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.