Mojo Max Fusion XXX, 500 mg, one capsule per blister card, 20 count box, Distributed by: Max Nutr...

FDA Recall #D-0396-2026 — Class I — October 8, 2025

Recall #D-0396-2026 Date: October 8, 2025 Classification: Class I Status: Ongoing

Product Description

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 for Recall

Marketed Without an Approved NDA/ANDA-FDA analysis revealed undeclared sildenafil (13.1 mg/capsule) and tadalafil (13.8 mg/capsule).

Recalling Firm

Mohamed Hagar — Brooklyn Ctr, MN

Classification

Class I — Reasonable probability of serious adverse health consequences or death.

Product Type

Drugs

Product Quantity

125 boxes

Distribution

U.S. Nationwide

Code Information

ALL LOTS, exp 12/31/2027

Status

Ongoing

Voluntary / Mandated

Voluntary: Firm initiated