Terminated Class II

Sunset Natural Products Inc.

Recall F-0544-2016 · Miami, FL

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

Quantity affected

100,000 capsules

Recall type

FDA Mandated

Lot / code info

Lot # 160614 Exp. Date 06/17 and Lot # 490914 Exp. Date 10/17

Timeline

5 Oct 2015 initiated 17 Feb 2016 classified 24 Feb 2016 reported 10 Apr 2017 terminated

Sourced directly from the FDA’s openFDA enforcement database. This information is for educational purposes only and does not constitute health or legal advice. FoodRecallFinder.com is not affiliated with or endorsed by the U.S. Food and Drug Administration.