Golden State Medical Supply Inc. recalls Primidone Tablets
- Recalling company
- Golden State Medical Supply Inc.
- Product
- 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
- Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.
- Classification
- Class III – not likely to cause adverse health consequences
- Recall date
- Apr 27, 2026
- Reported
- May 27, 2026
- Distribution
- USA Nationwide
- Status
- Ongoing
- Quantity
- 1,620 bottles
- Lot / codes
- Lot #: GS067909, Exp 4/30/2028; GS068646, Exp 8/31/2026
- Company location
- Camarillo, CA
- Recall type
- Voluntary: Firm initiated
- Recall number
- D-0535-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number D-0535-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.