WhichRecall
Class I — UrgentReported 2025-01-08

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

Recalled by GNMart LLC

Reason for Recall

Marketed without an approved NDA/ANDA

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FDA analysis found the product to be tainted with Diclofenac and Dexamethasone.

Recall Number
D-0170-2025
Classification
Class I
Status
Ongoing
Category
drug
Initiated
2024-12-12
Reported
2025-01-08
Distribution
Nationwide within the United States
Code Info
All lots, Exp. Date: 03/27/2030
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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