Recall RadarFexofenadine Hydrochloride Tablets, USP 180 mg, Antihistamine, 150 Tablets per bottle, Distributed by: Ohm Laboratories, Inc., New Brunswick, NJ 08901. NDC 66336-561-30
Failed Impurities/Degradation Specifications
Read the official FDA notice →What to do
Stop using the product and check it against the description above. Follow the remedy on the official notice; most recalls are refunded or replaced without a receipt. If you or a family member has already been affected, keep the packaging and the lot code — they're what a claim rests on later.
Details
- Recalling company
- SUN PHARMACEUTICAL INDUSTRIES INC — Princeton, NJ
- Severity
- Class III — low
- Reported
- July 8, 2026
- Quantity
- 9,048 bottles
- Recall number
- D-0654-2026
- Status
- Ongoing
- Source
- FDA
Where it went
U.S. Nationwide
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