← FDA ENFORCEMENT
D-0170-2025Class I

GNMart LLC

Recalling firm
GNMart LLC
Product type
Drug
Status
Ongoing
Report date
2025-01-08
Distribution
Nationwide within the United States
Firm state
NY
Product quantity
374 bottles
Initiated by
Voluntary: Firm initiated
Reason for recall

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

Product description

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

Code / lot info

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

Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.