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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

Mojo Max Fusion XXX Recalled for Undeclared Drug Ingredients

Agency Publication Date: March 5, 2026
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Summary

Mohamed Hagar is recalling 125 boxes of Mojo Max Fusion XXX (500 mg) capsules because FDA laboratory analysis found they contain undeclared sildenafil and tadalafil. These ingredients are the active medications in FDA-approved prescription drugs used to treat erectile dysfunction, but they are not listed on the product packaging. The recall affects all lots of the 20-count boxes, which contain one capsule per blister card, distributed nationwide by Max Nutrition Inc.

Risk

These undeclared ingredients can pose a serious health risk because they may interact with nitrates found in some prescription drugs (such as nitroglycerin), potentially lowering blood pressure to dangerous levels. Consumers with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates and are at particular risk.

What You Should Do

  1. Check your packaging for Mojo Max Fusion XXX, 500 mg, sold in a 20-count box with UPC 6 78945 36675 0.
  2. Verify if you have any products from ALL LOTS with an expiration date of 12/31/2027.
  3. 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 Mohamed Hagar for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions or to report adverse effects.

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: Mojo Max Fusion XXX (500 mg)by Mojo Max Fusion XXX
Variants: 500 mg, one capsule per blister card, 20 count box
UPC Codes:
678945366750
Lot Numbers:
ALL LOTS (exp 12/31/2027)

Distributed by Max Nutrition Inc.; Recall #: D-0396-2026

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 97796
Status: Active
Manufacturer: Mohamed Hagar
Sold By: Max Nutrition Inc.
Manufactured In: United States
Units Affected: 125 boxes
Distributed To: Nationwide
Agency Last Updated: March 17, 2026

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 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.