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Class II · ModerateRecall completed

LISINOPRIL AND HYDROCHLOROTHIAZIDE TABLETS

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

Does this affect you?
Check your lot numberExp NDC Lot # Date [redacted-phone] 69393A1 09/2015 [redacted-phone]-1 0 69395A1 09/2015 [redacted-phone] 69495A1 10/2015 [redacted-phone] 69496A1 10/2015 [redacted-phone] 69497A1 02/2014 [redacted-phone] 69524A1 10/2015 [redacted-phone] 69524A2 10/2015 [redacted-phone] 69525A1 10/2015 [redacted-phone] 69525A2 10/2015
Where it was soldNationwide
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: Reports of gray smudges identified as minute stainless steel particulates were found in the recalled tablets by the manufacturer

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 / forGsms
NDC60429-046-01
Show the full FDA record
Full product labelLISINOPRIL AND HYDROCHLOROTHIAZIDE TABLETS, USP, 20 mg/25 mg, 100 (NDC 60429-046-01) and 1,000 (NDC 60429-046-10) count bottles, Rx only, GSMS Inc., Camarillo, CA
Recalling firmGsms
DistributionNationwide
Quantity6158 bottles
Recall initiated2013-03-11
Report date2013-04-17
Recall completed2013-09-03
Recall numberD-244-2013
ClassificationClass II
FDA statusTerminated
Origin on fileCamarillo CA United States

Related

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.