PlainRecalls
FDA Drug Critical Class I Terminated

Rhino 7 Platinum 3000, 1 count Blister Pack, Distributed by Rhino 7, Made in USA, UPC 700729253748

Reported: March 16, 2016 Initiated: September 25, 2015 #D-0772-2016

Product Description

Rhino 7 Platinum 3000, 1 count Blister Pack, Distributed by Rhino 7, Made in USA, UPC 700729253748

Reason for Recall

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

Details

Recalling Firm
Tf Supplements
Units Affected
128 Blister Packs
Distribution
Nationwide
Location
Houston, TX

Frequently Asked Questions

What product was recalled?
Rhino 7 Platinum 3000, 1 count Blister Pack, Distributed by Rhino 7, Made in USA, UPC 700729253748. Recalled by Tf Supplements. Units affected: 128 Blister Packs.
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-0772-2016.