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Class IOngoing

FORCE FOREVER 400mg Tablets recall

FDA recall D-0170-2025 · initiated Dec 12, 2024

By the pharmaranks editorial teamReviewed against the FDA (openFDA) sourcesUpdated Jan 8, 2025How we research

GNMart LLC recalled FORCE FOREVER 400mg Tablets in Dec 2024 — an FDA Class I recall (D-0170-2025) because Marketed without an approved NDA/ANDA. FDA analysis found the product to be tainted with Diclofenac and Dexamethasone.

Most serious — a reasonable probability that use will cause serious harm or death.

Why it was recalled

Marketed without an approved NDA/ANDA. FDA analysis found the product to be tainted with Diclofenac and Dexamethasone.

Sold unapproved, or found to contain something undeclared

The product should not have been on sale in this form — often a supplement found to contain a hidden prescription drug.

This is a manufacturing or quality failure, not a finding that the medicine is unsafe to take — across every recall we hold, none was issued for that reason. It does not mean the batch was harmless.

Is your product affected? Check the lot number

A recall covers only specific lots. Find the lot number and expiration date on your package and compare them to the affected codes below — if yours is not listed, it was not part of this recall.

All lots, Exp. Date: 03/27/2030

Quantity recalled: 374 bottles

Details

Product
FORCE FOREVER 400mg Tablets, Huesos y articulaciones sin dolor, SUPLEMENTO ALIMENTICIO, 60-count bottles
Recalling company
GNMart LLC
Classification
Class I
Status
Ongoing
Type
Voluntary: Firm initiated
Distribution
Nationwide within the United States
Initiated
Dec 12, 2024
FDA report date
Jan 8, 2025
What to do.If you have a recalled product, don't throw away questions — check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This page reproduces public FDA data and is not medical advice.

Frequently asked

Was FORCE FOREVER 400mg Tablets recalled?
GNMart LLC recalled FORCE FOREVER 400mg Tablets in Dec 2024 — an FDA Class I recall (D-0170-2025) because Marketed without an approved NDA/ANDA. FDA analysis found the product to be tainted with Diclofenac and Dexamethasone. Most serious — a reasonable probability that use will cause serious harm or death.
Why was FORCE FOREVER 400mg Tablets recalled?
Per the FDA enforcement record, the reason for recall D-0170-2025 was: Marketed without an approved NDA/ANDA. FDA analysis found the product to be tainted with Diclofenac and Dexamethasone.
Is a recalled FORCE FOREVER 400mg Tablets dangerous to take?
An FDA recall removes specific lots from the market for a defined reason and does not by itself mean the medicine is unsafe for everyone — your specific lot may never have been affected. Most serious — a reasonable probability that use will cause serious harm or death. Check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This reproduces public FDA data and is not medical advice.
Which lots of FORCE FOREVER 400mg Tablets are affected?
Distributed: Nationwide within the United States. The recall covers these lots — All lots, Exp. Date: 03/27/2030. Check the lot number and expiration date on your package against this list; if yours is not listed, it was not part of recall D-0170-2025.

Source: openFDA Drug Enforcement record D-0170-2025

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