FindMyRecallSubscribe
Class I: serious health riskOngoing

GNMart FORCE FOREVER 400mg Tablets Recall

FORCE FOREVER 400mg Tablets, Huesos y articulaciones sin dolor, SUPLEMENTO ALIMENTICIO,…

GNMart LLC · Dover Plains, NY

Risk level
Class I
Reported by FDA
Jan 8, 2025
Recall ID
D-0170-2025
Check your lot numberHow we source this data

Summary

GNMart recalled FORCE FOREVER 400mg Tablets starting Dec 12, 2024. The FDA classified it as Class I (serious health risk) and published enforcement report D-0170-2025 on Jan 8, 2025. Reason: Marketed without an approved NDA/ANDA. FDA analysis found the product to be tainted with Diclofenac and Dexamethasone. Status: Ongoing.

Why it was recalled

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

Product description

FORCE FOREVER 400mg Tablets, Huesos y articulaciones sin dolor, SUPLEMENTO ALIMENTICIO, 60-count bottles

Lot numbers, UPCs & expiration codes

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

Where it was sold

Nationwide within the United States

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0170-2025
Classification
Class I
Status
Ongoing
Recall initiated
Dec 12, 2024
FDA report date
Jan 8, 2025
Quantity
374 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
GNMart LLC

Original FDA data

Every field from FDA enforcement report D-0170-2025, exactly as published.

Show all FDA fields
City
Dover Plains
State
NY
Status
Ongoing
Country
United States
Event ID
96001
Address
7 Sawmill Ln
Code information
All lots, Exp. Date: 03/27/2030
Postal code
12522-6086
Report date
Jan 8, 2025
Product type
Drugs
Recall number
D-0170-2025
Classification
Class I
Recalling firm
GNMart LLC
Product quantity
374 bottles
Reason for recall
Marketed without an approved NDA/ANDA. FDA analysis found the product to be tainted with Diclofenac and Dexamethasone.
Voluntary / mandated
Voluntary: Firm initiated
Product description
FORCE FOREVER 400mg Tablets, Huesos y articulaciones sin dolor, SUPLEMENTO ALIMENTICIO, 60-count bottles
Distribution pattern
Nationwide within the United States
Recall initiation date
Dec 12, 2024
Initial firm notification
Press Release
Center classification date
Jan 2, 2025

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0170-2025, published Jan 8, 2025. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

How we source and update recall data · Report incorrect information

Other recent drug recalls