FlaggedRx← Medication recall checkHome
Class II · ModerateRecall completed

Lisinopril Tablets

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

Does this affect you?
Check your lot numberLot # a) C0570215B; Exp 02/17 b) C0570215A; Exp 02/17
Where it was soldNationwide and Puerto Rico
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

Failed Dissolution Specifications

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 / forQualitest Pharmaceuticals, Huntsville, AL 35811
NDC0603-4214-60
Show the full FDA record
Full product labelLisinopril Tablets, USP, 40 mg, a) 45-count bottle (NDC 0603-4214-60), b) 500-count bottle (NDC 0603-4214-28), Rx Only, Manufactured for: Qualitest Pharmaceuticals, Huntsville, AL 35811
Recalling firmVintage Pharmaceuticals LLC dba Qualitest Pharmaceuticals
DistributionNationwide and Puerto Rico
Quantity8,705 bottles
Recall initiated2015-07-29
Report date2015-09-09
Recall completed2016-03-29
Recall numberD-1406-2015
ClassificationClass II
FDA statusTerminated
Origin on fileHuntsville AL 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.