HIGHFDA DRUG

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...

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.

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DRUG
Recall date
May 29, 2026
Status
ACTIVE

Quick Facts at a Glance

Recall Date
May 29, 2026
Hazard Level
HIGH
Brands
NIACIN, Golden State Medical Supply, Inc.

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Drug Safety; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
NIACIN, Golden State Medical Supply, Inc.
Model numbers
Lots: GS065128, GS065844, GS066695, GS067432, GS067993, expires: 01/31/2027.
UPC codes
51407-267, 51407-268, 51407-267-90, 51407-268-90

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    May 29, 2026

  2. Reported by FDA DRUG

    June 17, 2026

  3. RecallRadar source check

    June 23, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

Hazard Information

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.

What You Should Do

Consumers and healthcare providers should stop using this product immediately. Contact Golden State Medical Supply Inc. or your healthcare provider for guidance. Notification method: E-Mail

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Full Description

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.. Generic: NIACIN; Brand: NIACIN. 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. Quantity: 2,961 bottles. Distribution: Within the U.S Market.

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: How to Get Refunds and Replacements

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Product Classification

Product Details

Model Numbers
Lots: GS065128
GS065844
GS066695
GS067432
GS067993
+1 more
UPC Codes
51407-267
51407-268
51407-267-90
+1 more
Report Date
June 17, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE