Class I
Drug Recall: Mojo Max Fusion XXX, 500 mg, one capsule per blister card, 20 count box, Distributed by: Max Nutrition Inc. UPC 6 78945 36675 0
Mohamed Hagar · October 8, 2025
Reason for Recall
Marketed Without an Approved NDA/ANDA-FDA analysis revealed undeclared sildenafil (13.1 mg/capsule) and tadalafil (13.8 mg/capsule).
Distribution
U.S. Nationwide
States Affected
NATIONWIDE
Quantity Affected
125 boxes
Source: FDA (openFDA Drug Enforcement)
Recall number: D-0396-2026
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.