FDAFDA · Food and drugs·Recall number D-0672-2016
Rhino 7 3000, 6 count Bottle, Distributed by Rhino 7, Made in USA
Published February 24, 2016 · Recall initiated: September 30, 2015
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Marketed without an Approved NDA/ANDA: Products contain undeclared active pharmaceutical ingredients; desmethyl carbondenafil and dapoxetine.
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Manufacturer
- Premiere Sales Group
- Distributor
- Nationwide
- Lot
- All lots
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
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