# FDA recall F-0544-2016

> **Sunset Natural Products Inc.** · Class II · food recall initiated 2015-10-05.

## Product

Venocell, sold in bulk of 50,000 capsules.

## Reason for recall

Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufatured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.

## Distribution

FL and NV

## Key facts

- **Recall number:** F-0544-2016
- **Recalling firm:** Sunset Natural Products Inc.
- **Classification:** Class II
- **Product type:** food
- **Status:** Terminated
- **Initiation date:** 2015-10-05
- **Report date:** 2016-02-24
- **Termination date:** 2017-04-10

- **Voluntary/Mandated:** FDA Mandated
- **Location:** Miami, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=F-0544-2016

## Citation

> AI Analytics. FDA recall F-0544-2016. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/F-0544-2016. Source: US FDA. Licensed CC0.

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