Mojo Max Fusion XXX Capsules: Undeclared Sildenafil and Tadalafil Risk
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.
Recall notice
Marketed Without an Approved NDA/ANDA-FDA analysis revealed undeclared sildenafil (13.1 mg/capsule) and tadalafil (13.8 mg/capsule).
Contact the company
What happened, in plain English
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. Read more at govinfonow.com/recall/31748-mojo-max-fusion-xxx-capsules-undeclared-sildenafil-and-tadalafil-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/31748-mojo-max-fusion-xxx-capsules-undeclared-sildenafil-and-tadalafil-risk · Updated August 17, 2026 · FDA enforcement record: FDA #D-0396-2026
Cite this page
“Mojo Max Fusion XXX Capsules: Undeclared Sildenafil and Tadalafil Risk.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/31748-mojo-max-fusion-xxx-capsules-undeclared-sildenafil-and-tadalafil-risk. Based on FDA recall #D-0396-2026 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0396-2026%22&limit=1).
Why it’s dangerous
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.
Who’s affected
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.
How to tell if you have this one
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.
- Brand
Mohamed Hagar- Product
Mojo Max Fusion XXX, 500 mg, one capsule per blister card, 20 count box, Distributed by: Max Nutrition Inc. UPC 6 78945- Category
Drug
What to do — step by step
Check Product Details
Look for the product name 'Mojo Max Fusion XXX', 500 mg capsules, 20-count box, and UPC 678945 on the packaging.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “U.S. Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 5 months after the firm started it.
- Firm started the recall
- Published in FDA’s Enforcement Report
- FDA classified it Class I
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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.
- Official source: FDA Recall #D-0396-2026 (October 8, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0396-2026 to see it in context.
- Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.