Home Recalls D-0533-2026
Class III · Low risk Ongoing Initiated Apr 24, 2026 (4 months ago)
Primidone Tablets USP, 250mg, 100-count bottle, Rx only, Distributed by: Lannett Company…
Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
Why it was recalled
Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.
What was recalled
Primidone Tablets USP, 250mg, 100-count bottle, Rx only, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136, NDC 0527-1231-01.
Recalling firm Lannett Company Inc.
NDC code 0527-1231-01
Origin IN, United States
Initiated by Voluntary: Firm initiated
FDA recall number D-0533-2026
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.
Class III · Low risk Ongoing Jun 3, 2026
Reason Cross Contamination with Other Products: due to a potential for cross-contamination with Acemetacin API due to an issue at the API manufacturer.
Class III · Low risk Ongoing May 1, 2026
Reason Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.
Class III · Low risk Ongoing May 1, 2026
Reason Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.
Class III · Low risk Ongoing Apr 27, 2026
Reason Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.
Class III · Low risk Ongoing Apr 27, 2026
Reason Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.