Rhino 7 Platinum 3000 recalled over undeclared active
- Recall date
- September 30, 2015
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Premiere Sales Group recalls Rhino 7 Platinum 3000, 1 count Blister Pack, Distributed by Rhino 7, Made in USA
- Recall number
- D-0673-2016
- FDA classification
- Class I
- Brand / firm
- Premiere Sales Group
- Sold / distributed
- Nationwide
Why it was recalled
Marketed without an Approved NDA/ANDA: Products contain undeclared active pharmaceutical ingredients; desmethyl carbondenafil and dapoxetine.
Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.
What was recalled
Rhino 7 Platinum 3000, 1 count Blister Pack, Distributed by Rhino 7, Made in USA
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