FDA Drugs recall ·
FORCE FOREVER 400mg Tablets, Huesos y articulaciones sin dolor… recall
This is an FDA Class I recall — the most serious type.
Read the official FDA notice ↗
Product
FORCE FOREVER 400mg Tablets, Huesos y articulaciones sin dolor, SUPLEMENTO ALIMENTICIO, 60-count bottles
Why was it recalled?
Marketed without an approved NDA/ANDA. FDA analysis found the product to be tainted with Diclofenac and Dexamethasone.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
All lots, Exp. Date: 03/27/2030
Distribution
Nationwide within the United States
What does Class I mean?
Class I is the most serious FDA recall class: there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
Source: FDA (drugs), recall D-0170-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.