FDA DrugClass IINotable

FDA Recall: Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphe

Date: 2026-07-08
Brand: Lannett Company Inc.
Category: Drug
FDA Class: Class II

Description

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

Hazard

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

Remedy

1392 bottles

View original recall →
Share:

Related Recalls

2026-06-10 · FDA_DRUG
FDA Recall: Niacin Extended-release Tablets, USP, 1,000 mg, 90-count bottles, Rx Only, Distributed by: Lannett C
Lannett Company Inc.
2026-05-27 · FDA_DRUG
FDA Recall: Primidone Tablets USP, 250mg, 100-count bottle, Rx only, Distributed by: Lannett Company, Inc., Phil
Lannett Company Inc.