PlainRecalls
FDA Drug Critical Class I Terminated

Rhino 7 Platinum 3000, 1 count Blister Pack, Distributed by Rhino 7, Made in USA

Reported: February 24, 2016 Initiated: September 30, 2015 #D-0673-2016

Product Description

Rhino 7 Platinum 3000, 1 count Blister Pack, Distributed by Rhino 7, Made in USA

Reason for Recall

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

Details

Recalling Firm
Premiere Sales Group
Distribution
Nationwide
Location
Santa Clarita, CA

Frequently Asked Questions

What product was recalled?
Rhino 7 Platinum 3000, 1 count Blister Pack, Distributed by Rhino 7, Made in USA. Recalled by Premiere Sales Group.
Why was this product recalled?
Marketed without an Approved NDA/ANDA: Products contain undeclared active pharmaceutical ingredients; desmethyl carbondenafil and dapoxetine.
Which agency issued this recall?
This recall was issued by the FDA Drug on February 24, 2016. Severity: Critical. Recall number: D-0673-2016.