FDA Drugs recall ·
Mojo Max Fusion XXX, 500 mg, one capsule per blister card, 20 count box… recall
This is an FDA Class I recall — the most serious type.
- Recall number
- D-0396-2026
- Date
- (initiated October 8, 2025)
- Company / brand
- Mohamed Hagar
4952 Highway 169 N, Brooklyn Ctr, MN, United States - Category
- Drugs › Class I
- Classification
- Class I
- Status
- Ongoing
- Units affected
- 125 boxes
- Hazard tags
- Undeclared allergen
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
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
Why was it recalled?
Marketed Without an Approved NDA/ANDA-FDA analysis revealed undeclared sildenafil (13.1 mg/capsule) and tadalafil (13.8 mg/capsule).
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
ALL LOTS, exp 12/31/2027
Distribution
U.S. Nationwide
What does Class I mean?
Class I is the most serious FDA recall class: there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
Source: FDA (drugs), recall D-0396-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.