Golden State Medical Supply recalls NIACIN Extended-Release Tablets (1000mg) manufactured by Kremers Urban due to failed dissolution specifications. This may affect prescription medication safety.
Failed Dissolution Specifications
Golden State Medical Supply is recalling NIACIN Extended-Release Tablets (1000mg) because they failed dissolution specifications. This means the tablets may not release medication properly, potentially causing unsafe drug levels in the body.
The tablets failed to dissolve correctly as intended, which could lead to inconsistent medication release. This might cause either too little or too much medication to be absorbed by the body, potentially affecting treatment effectiveness.
Prescription patients who have received this specific NIACIN tablet product. Those with medical conditions requiring precise medication dosing are most at risk.
Look for NIACIN Extended-Release Tablets, USP, 1000 mg, 90 tablets per bottle, prescription-only. The NDC code starts with 51407-268-90 and the lot numbers listed in the recall notice.
Verify the product name, strength, and packaging to confirm if it matches the recalled NIACIN Extended-Release Tablets (1000mg, 90 tablets per bottle).
Ask your pharmacist if you have the recalled product and whether they can help you get a replacement or alternative medication.
The tablets failed dissolution specifications, meaning they may not release medication properly, which could lead to inconsistent drug levels in the body.
Look for NIACIN Extended-Release Tablets, USP, 1000 mg, 90 tablets per bottle, prescription-only. The NDC code starts with 51407-268-90 and the lot numbers listed in the recall notice.
Contact your pharmacist to discuss options for getting a replacement or alternative medication.
We’ve drafted a message you can send Golden State Medical Supply to request your refund or repair — edit it as you like.
Subject: Recall D-0158-2026 — Golden State Medical Supply Golden State Medical Supply Hello, I own a Golden State Medical Supply that is covered by recall D-0158-2026 from Golden State Medical Supply. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
