Home / Food recalls / 2016
Sunset Natural Products Inc.
FDA recall F-0544-2016 · Class II · reported 2016-02-24 · Terminated
- Product
- Venocell, sold in bulk of 50,000 capsules.
- Reason
- 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.
- Quantity
- 100,000 capsules
- Distribution
- FL and NV
- Firm location
- FL, United States
- Initiated
- FDA Mandated
- First notice
- Other
- Recall started
- 2015-10-05
- Terminated
- 2017-04-10
- Code info
- Lot # 160614 Exp. Date 06/17 and Lot # 490914 Exp. Date 10/17
Source: U.S. Food and Drug Administration, openFDA Food Enforcement database (openFDA Food Enforcement, imported 2026-09). The FDA does not validate openFDA data for completeness or accuracy. This is a record of an enforcement action, not safety advice.