Class I โ€” Serious Health Hazard

Serious health hazard โ€” there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.

MOJO RISEN Recalled by Eugene Oregon, Inc. Due to Undeclared Sildenafil

Date: May 5, 2014
Company: Eugene Oregon, Inc.
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Eugene Oregon, Inc. directly.

Affected Products

MOJO RISEN, 650 mg, 2 capsule per pouch, Distributed by: Mojo Risen, LLC, Springville, UT 84663

Quantity: 57 boxes

Why Was This Recalled?

Marketed Without an Approved NDA/ANDA: Eugene FDA laboratory analyses determined they contain undeclared sildenafil.

Where Was This Sold?

This product was distributed to 11 states: FL, IL, IN, LA, ME, MD, NJ, PA, SC, TX, WA

Affected (11 states)Not affected

About Eugene Oregon, Inc.

Eugene Oregon, Inc. has 3 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report