Information
Golden State Medical Supply Inc. Recalls Primidone Tablets
This is a Class III recall. This product is unlikely to cause adverse health reactions but violates FDA regulations.
Source: FDA
InfoRecall #D-0535-2026Drug / Pharmaceutical
Golden State Medical Supply Inc. Recalls Primidone Tablets
Golden State Medical Supply Inc. · Class III — Regulatory
Product Description
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
Reason for Recall
Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.
FDA Classification
Class III — Regulatory
A situation in which use of, or exposure to, a violative product is not likely to cause adverse health consequences.
Distribution
USA Nationwide
Remedy
Consumers should stop using this product. Contact the recalling firm for further instructions regarding this product.
411 Press Analysis
Golden State Medical Supply Inc. initiated a Class III recall of a pharmaceutical product on April 27, 2026 affecting 1,620 bottles. Cross contamination with other products: API contaminated with trace amounts of Acemetacin API. Class III recalls involve products that are unlikely to cause adverse health reactions but violate FDA regulations. The product was distributed in USA Nationwide. Consumers may continue monitoring FDA updates regarding this recall.
Sources: FDA openFDA Enforcement Database
This recall appears in: Drug & Medical Product Contamination.