RecallRadar

FDA Drug recall D-0335-2019

infants* IBUPROFEN, Concentrated Ibuprofen Oral Suspension, USP (NSAID), 50 mg per 1.25 mL, Dye-Free Berry Flavor, 0.5 FL OZ (15 mL) bottle…

On 2018-12-26 the FDA classified a Class II recall of infants* IBUPROFEN, Concentrated Ibuprofen Oral Suspension, USP (NSAID), 50 mg per 1.25 mL, Dye-Free Berry Flavor, 0.5 FL OZ (15 mL) bottle… by Tris Pharma, citing superpotent Drug: recalled lots may have higher concentration of ibuprofen.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0335-2019
ClassificationClass II
Statusterminated
Initiated2018-11-26
Published2018-12-26
Last updated2026-09-13 11:52 UTC
CompanyTris Pharma
DistributionUS

Product

infants* IBUPROFEN, Concentrated Ibuprofen Oral Suspension, USP (NSAID), 50 mg per 1.25 mL, Dye-Free Berry Flavor, 0.5 FL OZ (15 mL) bottle, Distributed by Wal-Mart Stores, Inc., Bentonville, AR 72716, NDC 49035-125-23, UPC 0 78742 02016 7.

Reason

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

Identifiers

upc078742020167
code_infoLot #: 00717009A, Exp 02/19; 00717015A, Exp 04/19; 00717024A, Exp 08/19

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0335-2019%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.