D-0771-2016 Class I Terminated
FDA drug recall D-0771-2016 was initiated by Tf Supplements on September 25, 2015 and is designated Class I. Reason for recall: Marketed without an Approved NDA/ANDA: Products contain undeclared desmethyl carbondenafil and dapoxetine. The recall status is terminated (terminated May 19, 2022). Affected quantity: 350 Bottles.
Recall Details
- Product Type
- Drugs
- Report Date
- March 16, 2016
- Initiation Date
- September 25, 2015
- Termination Date
- May 19, 2022
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 350 Bottles
Product Description
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 Pattern
Nationwide
Code Information
All lots