Recall RadarPrimidone Tablets USP, 250mg, 100-count bottle, Rx only, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136, NDC 0527-1231-01.
Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.
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
- Lannett Company Inc. — Seymour, IN
- Severity
- Class III — low
- Reported
- May 27, 2026
- Quantity
- 44865 bottles
- Recall number
- D-0533-2026
- Status
- Ongoing
- Source
- FDA
Where it went
USA Nationwide
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