Recall RadarNiacin Extended-release Tablets, USP, 1,000 mg, 90-count bottles, Rx Only, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136, NDC 62175-322-46.
Failed Dissolution Specifications: during 12M LT stability testing OOS low for Stage 3 dissolution at the 24-hour timepoint.
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 II — moderate
- Reported
- June 10, 2026
- Quantity
- 3984 bottles
- Recall number
- D-0584-2026
- Status
- Ongoing
- Source
- FDA
Where it went
Nationwide within the United States
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