D-0170-2025 Class I Ongoing
FDA drug recall D-0170-2025 was initiated by GNMart LLC on December 12, 2024 and is designated Class I. Reason for recall: Marketed without an approved NDA/ANDA. FDA analysis found the product to be tainted with Diclofenac and Dexamethasone. The recall status is ongoing. Affected quantity: 374 bottles.
Recall Details
- Product Type
- Drugs
- Report Date
- January 8, 2025
- Initiation Date
- December 12, 2024
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 374 bottles
Product Description
FORCE FOREVER 400mg Tablets, Huesos y articulaciones sin dolor, SUPLEMENTO ALIMENTICIO, 60-count bottles
Reason for Recall
Marketed without an approved NDA/ANDA. FDA analysis found the product to be tainted with Diclofenac and Dexamethasone.
Distribution Pattern
Nationwide within the United States
Code Information
All lots, Exp. Date: 03/27/2030