Class I · Most seriousActive recall
Mojo Max Fusion XXX
A reasonable chance it could cause serious harm or death.
Does this affect you?
Check your lot numberALL LOTS, exp 12/31/2027
Where it was soldU.S. Nationwide
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.
What happened
Marketed Without an Approved NDA/ANDA-FDA analysis revealed undeclared sildenafil (13.1 mg/capsule) and tadalafil (13.8 mg/capsule).
What to do
- Check the lot number and expiry on your medicine against the recall above.
- Talk to your pharmacist or doctor before changing anything — don't stop on your own.
- Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).
Who makes it
| Distributed by / for | Max Nutrition Inc. UPC 6 78945 36675 0 |
Show the full FDA record
| Full product label | Mojo Max Fusion XXX, 500 mg, one capsule per blister card, 20 count box, Distributed by: Max Nutrition Inc. UPC 6 78945 36675 0 |
| Recalling firm | Mohamed Hagar |
| Distribution | U.S. Nationwide |
| Quantity | 125 boxes |
| Recall initiated | 2025-10-08 |
| Report date | 2026-03-11 |
| Recall completed | — |
| Recall number | D-0396-2026 |
| Classification | Class I |
| FDA status | Ongoing |
| Origin on file | Brooklyn Ctr MN United States |
Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗
This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.