FDA found undeclared sildenafil and tadalafil in Mojo Max Fusion XXX capsules. These drugs may cause serious health risks. Affected products include 20-count boxes with UPC 678945.
Marketed Without an Approved NDA/ANDA-FDA analysis revealed undeclared sildenafil (13.1 mg/capsule) and tadalafil (13.8 mg/capsule).
Mohamed Hagar recalled Mojo Max Fusion XXX capsules due to undeclared sildenafil and tadalafil. These ingredients could cause serious health issues if taken without proper medical supervision.
The capsules contain undeclared sildenafil (13.1 mg) and tadalafil (13.8 mg) without FDA approval. These drugs can interact with other medications or cause unexpected health effects if taken without medical guidance.
People who purchased the Mojo Max Fusion XXX capsules from stores or online are affected. Those with underlying health conditions or who take medications for erectile dysfunction may be at higher risk.
Check for the product name 'Mojo Max Fusion XXX', 500 mg capsules, 20-count box, and UPC 678945. The product was distributed by Max Nutrition Inc. and available from all lots until December 31, 2027.
Look for the product name 'Mojo Max Fusion XXX', 500 mg capsules, 20-count box, and UPC 678945 on the packaging.
The FDA found undeclared sildenafil (13.1 mg) and tadalafil (13.8 mg) in the product without proper approval.
The recall record does not specify a remedy, so contact Mohamed Hagar directly for guidance.
The product contains undeclared drugs that could cause health risks, so it is not safe to use without medical supervision.
We’ve drafted a message you can send Mohamed Hagar to request your refund or repair — edit it as you like.
Subject: Recall D-0396-2026 — Mohamed Hagar Mohamed Hagar Hello, I own a Mohamed Hagar that is covered by recall D-0396-2026 from Mohamed Hagar. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
