# FDA recall D-0673-2016

> **Premiere Sales Group** · Class I · drug recall initiated 2015-09-30.

## Product

Rhino 7 Platinum 3000, 1 count Blister Pack, Distributed by Rhino 7, Made in USA

## Reason for recall

Marketed without an Approved NDA/ANDA: Products contain undeclared active pharmaceutical ingredients; desmethyl carbondenafil and dapoxetine.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0673-2016
- **Recalling firm:** Premiere Sales Group
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2015-09-30
- **Report date:** 2016-02-24
- **Termination date:** 2017-06-01

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Santa Clarita, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0673-2016

## Citation

> AI Analytics. FDA recall D-0673-2016. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/D-0673-2016. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
