CLASS I Drug recall · Reported 16 Mar 2016 · FDA Enforcement Report
Rhino 7 3000, 6 count Bottle recalled by Tf Supplements
Tf Supplements is recalling Rhino 7 3000, 6 count Bottle, distributed nationwide in the US. The recall was initiated on 25 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-0771-2016
- FDA event ID
- 72294
- Recalling firm
- Tf Supplements, Houston, TX
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 25 Sep 2015
- FDA classified
- 9 Mar 2016
- Reported
- 16 Mar 2016
- Type
- Voluntary: Firm initiated
- Customers notified by
- Press Release
- Reason category
- Labeling Errors
Timeline
| 25 Sep 2015 | Recall initiated by company | |
| 9 Mar 2016 | Classified by FDA | +166 days |
| 16 Mar 2016 | Published in enforcement report | +7 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 desmethyl carbondenafil and dapoxetine.
Product as listed by the FDA
RHINO 7 3000, 6 count Bottle, Distributed by Rhino 7, Made in USA
Where it was distributed
Nationwide
Questions about this recall
Is Rhino 7 3000, 6 count Bottle recalled?
Yes. Tf Supplements recalled Rhino 7 3000, 6 count Bottle on 25 Sep 2015. The recall is Class I and its status is Terminated. Recall number D-0771-2016.
Why was it recalled?
Marketed without an Approved NDA/ANDA: Products contain undeclared 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 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from Tf Supplements
All 2| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS I | Rhino 7 Platinum recalled by Tf Supplements | Tf Supplements | Labeling Errors | Nationwide |