Recall RadarDextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate Extended-Release Capsules, 5 mg, Rx Only, 100 capsules, Distribu…
Labeling: Label Mix-up: Capsules contain only immediate-release (IR) pellets while labeled as ER capsules.
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
- July 8, 2026
- Quantity
- 1392 bottles
- Recall number
- D-0660-2026
- Status
- Ongoing
- Source
- FDA
Where it went
US Nationwide.
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