US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jan 15, 2019 (8 years ago)

infants* IBUPROFEN, Concentrated Ibuprofen Oral Suspension, USP (NSAID), 50 mg per 1.25…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Superpotent Drug: recalled lots may have higher concentration of ibuprofen than amount labeled.

What was recalled

infants* IBUPROFEN, Concentrated Ibuprofen Oral Suspension, USP (NSAID), 50 mg per 1.25 mL, Dye-Free Berry Flavor, 1 FL OZ (30 mL) bottle, Distributed by Wal-Mart Stores, Inc., Bentonville, AR 72716, NDC 49035-125-24.

Recalling firm
Tris Pharma Inc.
NDC code
49035-125-24
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0494-2019

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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