Dextroamphetamine/Amphetamine
FDA recalls
4 rows
| Date | Company and reason |
|---|---|
| Jun 25, 2026 | Lannett Company Inc. Labeling: Label Mix-up: Capsules contain only immediate-release (IR) pellets while labeled as ER capsules. |
| Aug 27, 2025 | Granules Pharmaceuticals Inc. Failed Impurities/Degradation Specifications: |
| Oct 8, 2020 | Ani Pharmaceuticals, Inc. Labeling: Incorrect expiration date. Product dated with 24-month expiration date instead of 18-months. |
| Feb 12, 2013 | Actavis Elizabeth LLC Failed Dissolution Specification: This product recall is due to the product lot # 50077231 exceeding dissolution specifications. All other test specifications were met. |
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Sources: CMS Medicare Part D Prescribers 2024; CMS Open Payments 2025 (general payments; a payment is not evidence of wrongdoing); FDA enforcement reports (openFDA).