FDA recall D-0771-2016
Tf Supplements · Class I · drug
Product
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.
Distribution
Nationwide
Key facts
- Status
- Terminated
- Initiation date
- 2015-09-25
- Report date
- 2016-03-16
- Termination date
- 2022-05-19
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Houston, TX, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0771-2016