CLASS I Drug recall · Reported 24 Feb 2016 · FDA Enforcement Report
Rhino 7 Platinum recalled by Premiere Sales Group
Premiere Sales Group is recalling Rhino 7 Platinum 3000, distributed nationwide in the US. The recall was initiated on 30 Sep 2015 and the FDA has classified it as Class I.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0673-2016
- FDA event ID
- 72522
- Recalling firm
- Premiere Sales Group, Santa Clarita, CA
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 30 Sep 2015
- FDA classified
- 16 Feb 2016
- Reported
- 24 Feb 2016
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Labeling Errors
Timeline
| 30 Sep 2015 | Recall initiated by company | |
| 16 Feb 2016 | Classified by FDA | +139 days |
| 24 Feb 2016 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Marketed without an Approved NDA/ANDA: Products contain undeclared active pharmaceutical ingredients; desmethyl carbondenafil and dapoxetine.
Product as listed by the FDA
Rhino 7 Platinum 3000, 1 count Blister Pack, Distributed by Rhino 7, Made in USA
Where it was distributed
Nationwide
Questions about this recall
Why was it recalled?
Marketed without an Approved NDA/ANDA: Products contain undeclared active pharmaceutical ingredients; desmethyl carbondenafil and dapoxetine.
Which lots are affected?
All lots
Where was it sold?
Nationwide
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
1 other product · FDA event 72522This product is part of a recall event; the main page for the event is Rhino 7 3000, 6 count Bottle recalled by Premiere Sales Group.
| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS I | Rhino 7 3000, 6 count Bottle recalled by Premiere Sales Group | Premiere Sales Group | Labeling Errors | Nationwide |
More recalls from Premiere Sales Group
All 2| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS I | Rhino 7 3000, 6 count Bottle recalled by Premiere Sales Group | Premiere Sales Group | Labeling Errors | Nationwide |