Golden State Medical Supply Inc.
14 federal recalls on file, showing the 6 from the last 12 months. We monitor every CPSC, FDA, USDA, and NHTSA notice for Golden State Medical Supply Inc. and translate it into plain English — free weekly digest, optional same-day alerts.
- 2026-09-09FDA-DrugNot Yet ClassifiedGolden State Medical Supply Prasugrel tablets recalled for dissolution failure
Golden State Medical Supply Inc. is recalling Prasugrel HCI 10mg tablets (lot GS062298, expiration 09/30/2026) because they failed to meet dissolution specifications during quality testing. Dissolution is how quickly a tablet breaks down in the body to release its active ingredient. Tablets that dissolve too slowly or incompletely may not work as intended.
- 2026-06-17FDA-DrugClass IIGolden State Medical Supply niacin tablets recalled for dissolution failure
Golden State Medical Supply is recalling specific lots of niacin extended-release tablets (1,000 mg) because they failed to dissolve properly during stability testing. The tablets did not meet dissolution specifications at the 24-hour mark, which means they may not release the medication as intended in the body.
- 2026-05-27FDA-DrugClass IIIGolden State Medical Supply Primidone Tablets recalled for contamination
Golden State Medical Supply's Primidone Tablets (250 mg) contain trace amounts of Acemetacin, a different medication, due to cross-contamination during manufacturing. This affects two lots distributed nationwide. No injuries have been reported.
- 2026-05-27FDA-DrugClass IIIGolden State Medical Supply Primidone recalled for API contamination
Golden State Medical Supply is recalling Primidone 50 mg tablets because the active ingredient was contaminated with trace amounts of Acemetacin, a different medication. This contamination occurred during manufacturing. The affected bottles are identified by specific lot numbers with expiration dates in 2028.
- 2025-12-24FDA-DrugClass IIStop using Golden State Medical Supply baclofen
Golden State Medical Supply's baclofen 10 mg tablets in 1,000-count bottles (Lot GS065762) may contain foreign tablets or capsules mixed in. This affects 2,472 bottles distributed nationwide. No injuries have been reported.
- 2025-11-26FDA-DrugClass IINIACIN Extended-Release Tablets, USP, 1,000 mg, 90 tablets per bottle, Rx only, Manufactured by: Kremers Urban Pharmaceuticals, Inc., a subsidiary of Lannett Company, Inc., Seymour, IN 47274. Packaged by GSMS, Incorporated, Carmarillo, CA 93012. NDC: 51407-268-90
Failed Dissolution Specifications
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