Home Recalls D-0535-2026
Class III · Low risk Ongoing Initiated Apr 27, 2026 (4 months ago)
Primidone Tablets, USP, 250 mg, 100-count bottle, RX only, Manufactured by: Lannett…
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, 250 mg, 100-count bottle, RX only, Manufactured by: Lannett Company, Inc., Marketed by: GSMS, Incorporated, Camarillo, CA 93012. NDC 51407-638-01
Recalling firm Golden State Medical Supply Inc.
NDC code 51407-638-01
Origin CA, United States
Initiated by Voluntary: Firm initiated
FDA recall number D-0535-2026
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 24, 2026
Reason Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.