US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Jun 26, 2026 (2 months ago)

Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Labeling: Label Mix-up: Capsules contain only immediate-release (IR) pellets while labeled as ER capsules.

What was recalled

Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate Extended-Release Capsules, 5 mg, Rx Only, 100 capsules, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136, NDC: 0527-0790-37.

Recalling firm
Lannett Company Inc.
Origin
IN, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0660-2026

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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