Mojo Max Fusion XXX recall
FDA recall D-0396-2026 · initiated Oct 8, 2025
Mohamed Hagar recalled Mojo Max Fusion XXX in Oct 2025 — an FDA Class I recall (D-0396-2026) because Marketed Without an Approved NDA/ANDA-FDA analysis revealed undeclared sildenafil (13.1 mg/capsule) and tadalafil (13.8 mg/capsule).
Most serious — a reasonable probability that use will cause serious harm or death.
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).
Sold unapproved, or found to contain something undeclared
The product should not have been on sale in this form — often a supplement found to contain a hidden prescription drug.
This is a manufacturing or quality failure, not a finding that the medicine is unsafe to take — across every recall we hold, none was issued for that reason. It does not mean the batch was harmless.
Is your product affected? Check the lot number
A recall covers only specific lots. Find the lot number and expiration date on your package and compare them to the affected codes below — if yours is not listed, it was not part of this recall.
Quantity recalled: 125 boxes
Details
- 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
- Recalling company
- Mohamed Hagar
- Classification
- Class I
- Status
- Ongoing
- Type
- Voluntary: Firm initiated
- Distribution
- U.S. Nationwide
- Initiated
- Oct 8, 2025
- FDA report date
- Mar 11, 2026
Frequently asked
- Was Mojo Max Fusion XXX recalled?
- Mohamed Hagar recalled Mojo Max Fusion XXX in Oct 2025 — an FDA Class I recall (D-0396-2026) because Marketed Without an Approved NDA/ANDA-FDA analysis revealed undeclared sildenafil (13.1 mg/capsule) and tadalafil (13.8 mg/capsule). Most serious — a reasonable probability that use will cause serious harm or death.
- Why was Mojo Max Fusion XXX recalled?
- Per the FDA enforcement record, the reason for recall D-0396-2026 was: Marketed Without an Approved NDA/ANDA-FDA analysis revealed undeclared sildenafil (13.1 mg/capsule) and tadalafil (13.8 mg/capsule).
- Is a recalled Mojo Max Fusion XXX dangerous to take?
- An FDA recall removes specific lots from the market for a defined reason and does not by itself mean the medicine is unsafe for everyone — your specific lot may never have been affected. Most serious — a reasonable probability that use will cause serious harm or death. Check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This reproduces public FDA data and is not medical advice.
- Which lots of Mojo Max Fusion XXX are affected?
- Distributed: U.S. Nationwide. The recall covers these lots — ALL LOTS, exp 12/31/2027. Check the lot number and expiration date on your package against this list; if yours is not listed, it was not part of recall D-0396-2026.