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Class II · ModerateActive recall

Ibuprofen

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

Does this affect you?
Check your lot numberLot: 7261973A, 7261974A, Exp 01/31/2027
Where it was soldU.S.A. Nationwide
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: the firm received complaints for a gel-like mass and black particles in the product.

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 byMade in India foreign manufacturer
Brand nameIBUPROFEN
Generic nameIBUPROFEN
Active ingredient(s)IBUPROFEN
Distributed by / forTaro Pharmaceuticals U.S.A., Inc., Hawthorne, NY 10532, Made in India
NDC51672-5321-8
Show the full FDA record
Full product labelChildren's Ibuprofen Oral Suspension, USP, 100 mg per 5mL, 4 FL OZ (120 mL) bottle, Manufactured for: Taro Pharmaceuticals U.S.A., Inc., Hawthorne, NY 10532, Made in India, NDC 51672-5321-8.
Recalling firmSTRIDES PHARMA INC
DistributionU.S.A. Nationwide
Quantity89592 bottles
Recall initiated2026-03-02
Report date2026-03-25
Recall completed—
Recall numberD-0390-2026
ClassificationClass II
FDA statusOngoing
Origin on fileBridgewater NJ United States

Related

Ibuprofen 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.