Dextroamphetamine Saccharate recall
Lannett Company Inc. recalled Dextroamphetamine Saccharate on July 8, 2026 because of labeling: Label Mix-up: Capsules contain only immediate-release (IR) pellets while labeled as ER capsules. It was sold nationwide.
Why it was recalled
Labeling: Label Mix-up: Capsules contain only immediate-release (IR) pellets while labeled as ER capsules.
What's 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.
Quantity: 1392 bottles
What to do
Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.
Read the official FDA noticeDetails
- Company
- Lannett Company Inc., Seymour, IN
- Date
- Severity
- Class II
the product could cause temporary or reversible health problems. - Where sold
- Nationwide
US Nationwide. - Status
- Ongoing
- Recall number
- D-0660-2026
- Source
- U.S. Food and Drug Administration
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