Drug recall
Rhino 7 3000, 6 count Bottle, Distributed by Rhino 7, Made in USA
FDA recall event 72522 · Class I · Premiere Sales Group
Key facts
| Event ID | 72522 |
|---|---|
| Recall numbers | D-0672-2016, D-0673-2016 |
| Recalling firm | Premiere Sales Group |
| Product type | Drugs |
| Products | Rhino 7 3000, 6 count Bottle, Distributed by Rhino 7, Made in USA, Rhino 7 Platinum 3000, 1 count Blister Pack, Distributed by Rhino 7, Made in USA |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Marketed without an Approved NDA/ANDA: Products contain undeclared active pharmaceutical ingredients; desmethyl carbondenafil and dapoxetine. |
| Initiation date | Sep 30, 2015 |
| Report date | Feb 24, 2016 |
| Termination date | Jun 1, 2017 |
| City | Santa Clarita |
| State | CA |
| Country | United States |
| FEI number | 3011888369 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: