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Class I: serious health riskOngoing

Mohamed Hagar Mojo Max Fusion XXX Recall

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

Mohamed Hagar · Brooklyn Ctr, MN

Risk level
Class I
Reported by FDA
Mar 11, 2026
Recall ID
D-0396-2026
Check your lot numberHow we source this data

Summary

Mohamed Hagar recalled Mojo Max Fusion XXX starting Oct 8, 2025. The FDA classified it as Class I (serious health risk) and published enforcement report D-0396-2026 on Mar 11, 2026. Reason: Marketed Without an Approved NDA/ANDA-FDA analysis revealed undeclared sildenafil (13.1 mg/capsule) and tadalafil (13.8 mg/capsule). Status: Ongoing.

Why it was recalled

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

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

Lot numbers, UPCs & expiration codes

ALL LOTS, exp 12/31/2027

Where it was sold

U.S. Nationwide

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0396-2026
Classification
Class I
Status
Ongoing
Recall initiated
Oct 8, 2025
FDA report date
Mar 11, 2026
Quantity
125 boxes
Recall type
Voluntary: Firm initiated
Recalling firm
Mohamed Hagar

Original FDA data

Every field from FDA enforcement report D-0396-2026, exactly as published.

Show all FDA fields
City
Brooklyn Ctr
State
MN
Status
Ongoing
Country
United States
Event ID
97796
Address
4952 Highway 169 N
Code information
ALL LOTS, exp 12/31/2027
Postal code
55428-4026
Report date
Mar 11, 2026
Product type
Drugs
Recall number
D-0396-2026
Classification
Class I
Recalling firm
Mohamed Hagar
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
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
Distribution pattern
U.S. Nationwide
Recall initiation date
Oct 8, 2025
Initial firm notification
E-Mail
Center classification date
Mar 17, 2026

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0396-2026, published Mar 11, 2026. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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