FDA Drug Recalls

Recalls / Class II

Class IID-0494-2019

Product

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.

Affected lot / code info
Lot#: 00717005A, Exp 02/19

Why it was recalled

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

Recalling firm

Firm
Tris Pharma Inc.
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
2033 US Highway 130, N/A, Monmouth Junction, New Jersey 08852-3003

Distribution

Quantity
35,328 bottles
Distribution pattern
One distributor who further distributed Nationwide in the USA.

Timeline

Recall initiated
2019-01-15
FDA classified
2019-02-14
Posted by FDA
2019-02-20
Terminated
2023-03-29
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0494-2019. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.

Class II recall: drug · FDA Drug Recalls