FDA DrugsClass I
Mojo Max Fusion XXX, 500 mg, one capsule per blister card, 20 count box, Distrib...
Published: March 11, 2026Recall ID: D-0396-2026Category: drugsCountry: US
Reason for Recall / Hazard
Marketed Without an Approved NDA/ANDA-FDA analysis revealed undeclared sildenafil (13.1 mg/capsule) and tadalafil (13.8 mg/capsule).
Product Description & Identification
Mojo Max Fusion XXX, 500 mg, one capsule per blister card, 20 count box, Distributed by: Max Nutrition Inc. UPC 6 78945 36675 0
Additional Source Details
| Field | Value |
|---|---|
| City | Brooklyn Ctr |
| State | MN |
| Event id | 97796 |
| Address 1 | 4952 Highway 169 N |
| Address 2 | N/A |
| Code info | ALL LOTS, exp 12/31/2027 |
| Postal code | 55428-4026 |
| Report date | 20260311 |
| Product type | Drugs |
| Product quantity | 125 boxes |
| Reason for recall | Marketed Without an Approved NDA/ANDA-FDA analysis revealed undeclared sildenafil (13.1 mg/capsule) and tadalafil (13.8 mg/capsule). |
| Voluntary mandated | Voluntary: Firm initiated |
| Recall initiation date | 20251008 |
| Initial firm notification | |
| Center classification date | 20260317 |
Overview
- Recalling FirmMohamed Hagar
- StatusOngoing
- Risk LevelClass I
- DistributionU.S. Nationwide