Golden State Medical Supply recalls
12 federal recalls on file, showing the 6 from the last 12 months. We read every CPSC, FDA, USDA and NHTSA notice for Golden State Medical Supply and put it in plain English.
Recent recalls
- Golden State prasugrel tablets recalled for failed dissolution
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.
ModerateFDASep 9, 20262 products
- Golden State Medical Supply carbamazepine recalled for black specks
Golden State Medical Supply is recalling Carbamazepine Tablets, USP 200mg due to black specks found in some tablets. This is a manufacturing quality issue. The affected lots were distributed nationwide.
ModerateFDAAug 26, 2026
- Golden 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.
ModerateFDAJun 17, 2026
- Golden State Medical Supply primidone tablets recalled for 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.
ModerateFDAMay 27, 20262 products
- Golden State Medical Supply baclofen recalled for foreign tablets
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.
ModerateFDADec 24, 2025
- NIACIN 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
FDANov 26, 2025