CLASS I ONGOING Drug recall · Reported 8 Jan 2025 · FDA Enforcement Report
Force Forever 400mg Tablets recalled by GNMart
GNMart is recalling Force Forever 400mg Tablets, Huesos y articulaciones sin dolor, Suplemento Alimenticio, distributed nationwide in the US. The recall was initiated on 12 Dec 2024 and the FDA has classified it as Class I.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0170-2025
- FDA event ID
- 96001
- Recalling firm
- GNMart, Dover Plains, NY
- Classification
- Class I
- Status
- Ongoing
- Recall initiated
- 12 Dec 2024
- FDA classified
- 2 Jan 2025
- Reported
- 8 Jan 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Press Release
- Reason category
- Hidden Drug Ingredients
Timeline
| 12 Dec 2024 | Recall initiated by company | |
| 2 Jan 2025 | Classified by FDA | +21 days |
| 8 Jan 2025 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Marketed without an approved NDA/ANDA. FDA analysis found the product to be tainted with Diclofenac and Dexamethasone.
Products marketed as supplements sometimes contain undeclared prescription drug ingredients such as sildenafil or sibutramine. These can interact dangerously with other medicines.
Product as listed by the FDA
FORCE FOREVER 400mg Tablets, Huesos y articulaciones sin dolor, SUPLEMENTO ALIMENTICIO, 60-count bottles
Where it was distributed
Nationwide within the United States
Questions about this recall
Why was it recalled?
Marketed without an approved NDA/ANDA. FDA analysis found the product to be tainted with Diclofenac and Dexamethasone.
Which lots are affected?
All lots, Exp. Date: 03/27/2030
Where was it sold?
Nationwide within the United States
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.