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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Critical RiskFDA Drug
Medications & Supplements/Dietary Supplements

Force Forever Joint Supplements Recalled for Drug Contamination

Agency Publication Date: January 2, 2025
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Summary

GNMart LLC is recalling approximately 374 bottles of Force Forever 400mg Tablets (Huesos y articulaciones sin dolor), marketed as a dietary supplement. FDA analysis discovered that the tablets are tainted with diclofenac and dexamethasone, which are prescription drugs not approved for use in this product. The recall affects all lots of the 60-count bottles with an expiration date of 03/27/2030.

Risk

The product contains undeclared diclofenac and dexamethasone, which can cause serious side effects including gastrointestinal bleeding, cardiovascular issues, and hormonal imbalances. These substances can also interact dangerously with other medications, potentially leading to life-threatening complications if taken without medical supervision.

What You Should Do

  1. The recalled products are 60-count bottles of Force Forever 400mg Tablets (Huesos y articulaciones sin dolor) with an expiration date of 03/27/2030. All lots of this product are affected.
  2. If you have health concerns, contact your healthcare provider or pharmacist. Return any unused product to the place of purchase for a refund, throw it away, or contact GNMart LLC for further instructions.
  3. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider or pharmacist for guidance, or return any unused product to the place of purchase for a refund
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away. For prescription medications, a DEA take-back location or pharmacy mail-back program is preferred when available.

Affected Products

Product: Force Forever 400mg Tablets (60-count)by Force Forever
Variants: Tablets, 400mg, 60-count
Lot Numbers:
All lots (Exp. 03/27/2030)

Marketed as Huesos y articulaciones sin dolor, SUPLEMENTO ALIMENTICIO.

Product Images

Image 1 โ€“ Labeling, Force Forever Dietary Supplement

Image 1 โ€“ Labeling, Force Forever Dietary Supplement

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 96001
Status: Active
Manufacturer: GNMart LLC
Manufactured In: United States
Units Affected: 374 bottles
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท FDA Press Release ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.