# FDA recall D-0771-2016

> **Tf Supplements** · Class I · drug recall initiated 2015-09-25.

## Product

RHINO 7 3000, 6 count Bottle, Distributed by Rhino 7, Made in USA

## Reason for recall

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

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0771-2016
- **Recalling firm:** Tf Supplements
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2015-09-25
- **Report date:** 2016-03-16
- **Termination date:** 2022-05-19

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Houston, TX, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0771-2016

## Citation

> AI Analytics. FDA recall D-0771-2016. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/D-0771-2016. Source: US FDA. Licensed CC0.

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