FDA Recall D-0170-2025

GNMart LLC · Dover Plains, NY

Class I — life-threatening Ongoing 518 days on record

Highest impact — Class I recall — FDA determination of strong likelihood of serious adverse health consequence or death. Distribution is nationwide and the recall remains in progress.

Product

FORCE FOREVER 400mg Tablets, Huesos y articulaciones sin dolor, SUPLEMENTO ALIMENTICIO, 60-count bottles

Lot / code: All lots, Exp. Date: 03/27/2030

Quantity: 374 bottles

Reason for recall

Marketed without an approved NDA/ANDA. FDA analysis found the product to be tainted with Diclofenac and Dexamethasone.

Recall record

Recall number: D-0170-2025
Classification: Class I
Status: Ongoing
Voluntary or mandated: Voluntary: Firm initiated
Firm notification: Press Release
Distribution: Nationwide within the United States
Recall initiated: 2024-12-12
Classified by FDA Center: 2025-01-02
FDA published: 2025-01-08
Recalling firm: GNMart LLC
Firm location: Dover Plains, NY

Operational response

A Class I recall indicates a strong likelihood of serious adverse health consequence or death. Pull affected lots from active dispensing immediately. Segregate inventory in a marked, locked location pending destruction or return. If product has already been dispensed, identify affected patients and contact them by your standard recall-notification protocol.

For the official FDA enforcement record, see FDA's Recall Search.

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