NIACIN Extended-Release Tablets — Class II drug recall D-0158-2026
Ongoing recall by Golden State Medical Supply Inc., reported 2025-11-26, distributed nationwide. Failed Dissolution Specifications
| Recall number | D-0158-2026 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Golden State Medical Supply Inc., Camarillo, CA, United States |
| Recall initiated | 2025-10-20 |
| Classified | 2025-11-19 |
| Reported by FDA | 2025-11-26 |
| Distributed | Nationwide (US) |
| Quantity | 24,869 bottles |
| Reason classes | specification failure |
| NDC | 51407-0267, 51407-0267-90, 51407-0268, 51407-0268-90 |
| Lot numbers | GS044385, GS044979, GS045797, GS046415, GS047197, GS047786, GS048477, GS048873, GS049480, GS049733, GS050224, GS050721, GS050722, GS051145, GS051726, GS052484, GS053612, GS054409, GS054987, GS055697, GS056192, GS056886, GS057330, GS058077 |
| Expiration dates | 2025-10, 2025-12, 2026-02, 2026-03, 2026-04, 2026-05 |
Product
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
Reason for recall
Failed Dissolution Specifications
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0158-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.