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Class II · ModerateActive recall

Ibuprofen Tablets

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

Does this affect you?
Check your lot numberLot: B0223H, Exp: 5/31/2026; C3023H, Exp: 9/30/2026.
Where it was soldCA and NV
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 Impurities/Degradation Specifications - at 18-month Stability testing

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 / forPreferred Pharmaceuticals, Inc.
NDC68788-9110-03
Show the full FDA record
Full product labelIbuprofen Tablets, USP 400mg, Generic for Motrin, Pkg Size: 30 tablets per bottle, Mfg: Dr. Reddy's Laboratories, Louisiana, Shreveport, NDC 68788-9110-03.
Recalling firmPreferred Pharmaceuticals, Inc.
DistributionCA and NV
Quantity266 bottles
Recall initiated2024-08-08
Report date2024-09-04
Recall completed
Recall numberD-0647-2024
ClassificationClass II
FDA statusOngoing
Origin on fileAnaheim 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.