← FDA ENFORCEMENT
D-0170-2025Class I
GNMart LLC
What this record is not
A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.
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. 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. Open the enforcement explorer →