Golden State Medical Supply Inc. recalls GSMS Incorporated
- Recalling company
- Golden State Medical Supply Inc.
- Product
- GSMS Incorporated, NIACIN EXTENDED-RELEASE TABLETS, USP, 1,000 MG, 90 tablets, Rx only, Manufactured by Kremers Urban Pharmaceuticals Inc., a subsidiary of Lannett, Inc., Seymour, IN 47274, Packaged by GSMS Incorporated, Camarillo, CA 93012. NDC 51407-268-90.
- Reason
- Failed Dissolution Specifications: During 12-month long-term stability testing, subject lot was out of specification (low) for stage 3 dissolution at the 24-hour timepoint.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- May 29, 2026
- Reported
- Jun 17, 2026
- Distribution
- Within the U.S Market.
- Status
- Ongoing
- Quantity
- 2,961 bottles
- Lot / codes
- Lots: GS065128, GS065844, GS066695, GS067432, GS067993, expires: 01/31/2027.
- Company location
- Camarillo, CA
- Recall type
- Voluntary: Firm initiated
- Recall number
- D-0587-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number D-0587-2026 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.