December 2024 FDA Recall Drug by Gnmart Llc
D-0170-2025 - Marketed without an approved NDA/ANDA. FDA analysis found the product to be tainted with Diclofenac and Dexamethasone.

This Class I drug recall was voluntarily initiated by Gnmart Llc on December 12, 2024 for the product Drug. The FDA reported the reason for recall as marketed without an approved nda/anda. fda analysis found the product to be tainted with diclofenac and dexamethasone.. The product was distributed Nationwide and the recall is currently ongoing.

Recall Number: D-0170-2025

Reason for Recall
Marketed without an approved NDA/ANDA. FDA analysis found the product to be tainted with Diclofenac and Dexamethasone.
Initiated
12-12-2024
Reported
01-08-2025
Quantity
374 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
96001
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Ongoing
Recalling Firm About Recalling Firm
The firm responsible for the recall.
GNMart LLC
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide within the United States
Product Description About Product Description
Full technical description of the product.
FORCE FOREVER 400mg Tablets, Huesos y articulaciones sin dolor, SUPLEMENTO ALIMENTICIO, 60-count bottles

Batch or Lot Expiration Information

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