PlainRecalls
FDA Drug Critical Class I Terminated

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

Reported: March 16, 2016 Initiated: September 25, 2015 #D-0771-2016

Product Description

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

Reason for Recall

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

Details

Recalling Firm
Tf Supplements
Units Affected
350 Bottles
Distribution
Nationwide
Location
Houston, TX

Frequently Asked Questions

What product was recalled?
RHINO 7 3000, 6 count Bottle, Distributed by Rhino 7, Made in USA. Recalled by Tf Supplements. Units affected: 350 Bottles.
Why was this product recalled?
Marketed without an Approved NDA/ANDA: Products contain undeclared desmethyl carbondenafil and dapoxetine.
Which agency issued this recall?
This recall was issued by the FDA Drug on March 16, 2016. Severity: Critical. Recall number: D-0771-2016.