Golden State Medical Supply Inc.: Gsms Incorporated, Niacin Extended-release Tablets, Usp, 1,000 Mg, 90 Tablets

Recall Summary Golden State Medical Supply Inc. is recalling GSMS Incorporated Niacin Extended-Release Tablets, 1,000 mg (90-tablet bottles, NDC 51407-268-90) distributed in the United States. The tablets failed to dissolve properly during stability testing, meaning they may not release the medication as intended in the body. This recall affects prescription niacin products manufactured by Kremers Urban Pharmaceuticals Inc. and packaged by GSMS Incorporated.

Recalling firm
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
Category
drug recall
Country
United States
Agency
U.S. Food and Drug Administration
Recall date
2026-05-29
Status
Ongoing
Distribution
Within the U.S Market.

Official recall notice from U.S. Food and Drug Administration

Recall details on Nibble Recalls: https://trynibble.app/recalls/cb1dbbf5-a512-468f-8555-3de550e04f45