Mohamed Hagar recalls Mojo Max Fusion XXX
- Recalling company
- 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 36675 0
- Reason
- Marketed Without an Approved NDA/ANDA-FDA analysis revealed undeclared sildenafil (13.1 mg/capsule) and tadalafil (13.8 mg/capsule).
- Classification
- Class I – a reasonable probability that use will cause serious adverse health consequences or death
- Recall date
- Oct 8, 2025
- Reported
- Mar 11, 2026
- Distribution
- U.S. Nationwide
- Status
- Ongoing
- Quantity
- 125 boxes
- Lot / codes
- ALL LOTS, exp 12/31/2027
- Company location
- Brooklyn Ctr, MN
- Recall type
- Voluntary: Firm initiated
- Recall number
- D-0396-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number D-0396-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.