Golden State Medical Supply Inc.: Drug Recall

Recall #D-0158-2026 · 10/20/2025

Class II: Risk

Recall Details

Recall Number: D-0158-2026
Classification: Class II
Product Type: Drug
Recalling Firm: Golden State Medical Supply Inc.
Status: Ongoing
Date Initiated: 10/20/2025
Location: Camarillo, CA, United States
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 24,869 bottles

Reason for Recall

Failed Dissolution Specifications

Product Description

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

Distribution Pattern

Nationwide in the USA

Other Recalls by Golden State Medical Supply Inc.

Class II: Risk 11/26/2025

Presence of Foreign Tablets/Capsules
Class II: Risk 03/05/2025

Failed Dissolution Specifications
Class II: Risk 05/13/2024

CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity (NDSRI), N-nitroso-duloxetine, above the proposed interim limit.
Class II: Risk 02/14/2024

CGMP Deviations:Suspected potential presence of Burkholderia cepacia complex
Class II: Risk 01/12/2024

Failed Dissolution Specifications

View all recalls by Golden State Medical Supply Inc. →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.