US Drug Recall Register
Class I · High risk Terminated Initiated Sep 30, 2015 (11 years ago)

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

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

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

What was recalled

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

Recalling firm
Premiere Sales Group
Origin
CA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0672-2016

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.