FORCE FOREVER 400mg Tablets, Huesos y articulaciones sin dolor, SUPLEMENTO ALIMENTICIO, 60-count bottles
Summary
The FDA issued a Class I for FORCE FOREVER 400mg Tablets, Huesos y articulaciones sin dolor, SUPLEMENTO ALIME by GNMart LLC. Reason: Marketed without an approved NDA/ANDA. FDA analysis found the product to be tainted with Diclofenac and Dexamethasone..
Details
Source
Drug Recall
External ID
D-0170-2025
Action Date
2025-01-08
Status
Ongoing
Category
drug
Product Description
FORCE FOREVER 400mg Tablets, Huesos y articulaciones sin dolor, SUPLEMENTO ALIMENTICIO, 60-count bottles
Lot/Code Info: All lots, Exp. Date: 03/27/2030
Quantity Affected: 374 bottles
Reason for Recall
Marketed without an approved NDA/ANDA. FDA analysis found the product to be tainted with Diclofenac and Dexamethasone.
Distribution
Nationwide within the United States
Type: Voluntary: Firm initiated
Recall Initiated: 2024-12-12
Company
Dover Plains, NY
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 31 drug recalls issued in the same week, part of 267 drug-related FDA actions this month.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (GNMart LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does GNMart LLC have FDA actions?
This is the only FDA action we have on record for GNMart LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "D-0170-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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