FreshRecalls

Lannett Company recalls

3 recent recalls on record for Lannett Company in CPSC, NHTSA, and FDA data as of July 24, 2026 at 1:09 AM UTC.

Models with recalls

Dextroamphetamine Saccharate (1)Niacin Extended-release Tablets (1)Primidone Tablets USP (1)

All Lannett Company recalls

FDA Class II · Drug · July 8, 2026

Dextroamphetamine Saccharate recall — Lannett Company Inc.

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

Official ID D-0660-2026 · Official record ↗

FDA Class II · Drug · June 10, 2026

Niacin Extended-release Tablets recall — Lannett Company Inc.

Failed Dissolution Specifications: during 12M LT stability testing OOS low for Stage 3 dissolution at the 24-hour timepoint.

Official ID D-0584-2026 · Official record ↗

FDA Class III · Drug · May 27, 2026

Primidone Tablets USP recall — Lannett Company Inc.

Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.

Official ID D-0533-2026 · Official record ↗

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Compiled from official public-domain government data. Last checked July 24, 2026 at 1:09 AM UTC.