Mohamed Hagar recalls Mojo Max Fusion XXX capsules over undeclared sildenafil and tadalafil
FDA testing found that Mojo Max Fusion XXX capsules contain sildenafil (13.1 mg per capsule) and tadalafil (13.8 mg per capsule), which are not declared, and the product is marketed without an approved NDA/ANDA.
What to do
The notice does not give instructions. Read the official notice for details.
Note from Recalled Today: Don't stop taking a prescribed medicine before you talk to your pharmacist or doctor.
Recall details
- Product
- Mojo Max Fusion XXX, 500 mg, one capsule per blister card, 20 count box, Distributed by: Max Nutrition Inc. UPC 6 78945 36675 0
- Company
- Mohamed Hagar
- Hazard
- Marketed Without an Approved NDA/ANDA-FDA analysis revealed undeclared sildenafil (13.1 mg/capsule) and tadalafil (13.8 mg/capsule).
- Units
- 125 boxes
- Where sold
- U.S. Nationwide
- FDA classification
- Class I · Ongoing
- Classified by FDA
- March 17, 2026
- Recall started
- October 8, 2025
- FDA enforcement report
- March 11, 2026
- Identifiers
- Codes: ALL LOTS, exp 12/31/2027
- FDA recall number: D-0396-2026
The headline, summary and steps above are written in plain English from the official notice below. Identifiers are copied exactly as the agency published them. Always check the official notice before you act.
Official notice
The notice's own wording from FDA.
- Product
- Mojo Max Fusion XXX, 500 mg, one capsule per blister card, 20 count box, Distributed by: Max Nutrition Inc. UPC 6 78945 36675 0
- Reason for recall
- Marketed Without an Approved NDA/ANDA-FDA analysis revealed undeclared sildenafil (13.1 mg/capsule) and tadalafil (13.8 mg/capsule).
- Classification
- Class I (Ongoing)
- Distribution
- U.S. Nationwide
- Quantity
- 125 boxes
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