FDA Drug · D-0396-2026

Mojo Max Fusion XXX, 500 mg, one capsule per blister card, 20 count box, Distributed by: Max Nutrition Inc. UPC 6 78945 36675 0

Class I · Ongoing

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

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Affected lots / codes — check yours against thisALL LOTS, exp 12/31/2027
Recalling firm
Mohamed Hagar, Brooklyn Ctr, MN
Classification
Class I (most serious — risk of serious harm)
Status
Ongoing
Quantity
125 boxes
Distribution
U.S. Nationwide
Recall initiated
October 8, 2025
Classified
March 17, 2026
Initiation
Voluntary: Firm initiated
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Official source. This record is published by the U.S. FDA through the openFDA enforcement database. View the unmodified government record:
https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0396-2026%22
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Important. Recalls target specific lots and codes — compare the affected lots above against your own product. This page reproduces public FDA data for readability; EveryRecall is independent and not affiliated with the FDA.
Check this brand across all 8 databases →