Mojo Max Fusion XXX recalled for undeclared sildenafil and tadalafil
Mojo Max Fusion XXX capsules contain hidden prescription drugs—sildenafil and tadalafil—that were not listed on the label. These are potent medications that can cause serious health problems, especially if you take other drugs or have certain heart or blood pressure conditions. The FDA has not approved this product for sale.
From the FDA notice · Read the official notice ↗
What to do
- Stop taking Mojo Max Fusion XXX immediately.
- Do not throw capsules in the trash or flush them down the toilet. Take them to a pharmacy for safe disposal.
- If you have taken this product and feel chest pain, difficulty breathing, or severe dizziness, call 911 or go to the nearest emergency room right away.
- Contact your doctor if you have any concerns about your health after using this product.
Is yours affected?
Compare your label or packaging with the recalled product.
- 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
- UPC codes
- 6789453667500
- 678945366750
- Sold in
- Nationwide
- Made for
- Adults
Details
- Units affected
- 125 boxes
- Illnesses reported
- None reported
- Manufactured in
- 4952 Highway 169 N, N/A, Brooklyn Ctr, MN, United States
- Classification
- Class I
- Recall number
- D-0396-2026
In the FDA's words
- 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 Marketed Without an Approved NDA/ANDA-FDA analysis revealed undeclared sildenafil (13.1 mg/capsule) and tadalafil (13.8 mg/capsule). ALL LOTS, exp 12/31/2027 Distribution: U.S. Nationwide Affected quantity: 125 boxes
- Hazard
- Marketed Without an Approved NDA/ANDA-FDA analysis revealed undeclared sildenafil (13.1 mg/capsule) and tadalafil (13.8 mg/capsule).