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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,…

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.

Class II Medicine & devices FDA June 17, 2026
Read the official FDA notice →

What to do

Stop using the product and check it against the description above. Follow the remedy on the official notice; most recalls are refunded or replaced without a receipt. If you or a family member has already been affected, keep the packaging and the lot code — they're what a claim rests on later.

Details

Recalling company
Golden State Medical Supply Inc. — Camarillo, CA
Severity
Class II — moderate
Reported
June 17, 2026
Quantity
2,961 bottles
Recall number
D-0587-2026
Status
Ongoing
Source
FDA

Where it went

Within the U.S Market.

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