Rhino 7 Platinum 3000 recalled over undeclared desmethyl

Recall date

September 25, 2015

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Official notice title

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

Recall number

D-0772-2016

FDA classification

Class I

Brand / firm

Tf Supplements

Sold / distributed

Nationwide

Why it was recalled

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

Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.

What was recalled

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