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.

Rhino 7 3000 Recalled by Premiere Sales Group Due to Undeclared Active

Date: September 30, 2015
Company: Premiere Sales Group
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 Premiere Sales Group directly.

Affected Products

Rhino 7 3000, 6 count Bottle, Distributed by Rhino 7, Made in USA

Quantity: 337 bottles

Why Was This Recalled?

Marketed without an Approved NDA/ANDA: Products contain undeclared active pharmaceutical ingredients; desmethyl carbondenafil and dapoxetine.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Premiere Sales Group

Premiere Sales Group has 2 total recalls tracked by RecallDetector.

Related Recalls

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