# FDA recall D-0396-2026

> **Mohamed Hagar** · Class I · drug recall initiated 2025-10-08.

## 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 for recall

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

## Distribution

U.S. Nationwide

## Key facts

- **Recall number:** D-0396-2026
- **Recalling firm:** Mohamed Hagar
- **Classification:** Class I
- **Product type:** drug
- **Status:** Ongoing
- **Initiation date:** 2025-10-08
- **Report date:** 2026-03-11

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Brooklyn Ctr, MN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0396-2026

## Citation

> AI Analytics. FDA recall D-0396-2026. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/D-0396-2026. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
