Sunset Natural Products Inc. Recall 72877
Description: Argindione, sold as bulk of 50,000 capsules.
Sunset Natural Products Inc. Recall 72877 Information
| Recall Status | Terminated |
| Recall Event ID | 72877 |
| Recall Number | F-0537-2016 |
| Recall Date | October 5, 2015 |
| Distribution | FL and NV |
| Quantity | 100,000 capsules |
| Recall Mandatory? | FDA Mandated |
| Product Type | Food |
| Food Classification | Class II |
| Recall 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. |
| Recalling Firm | Sunset Natural Products Inc. |
| Firm Address | 7345 SW 45th St Miami, FL, United States 33155-4509 |
| Inital Firm Notification | Other |
| Code Info | Lot # 480514 Exp. Date 05/17 and Lot # 320614 Exp. Date 06/17 |
| Report Date | February 24, 2016 |
| Classification Date | February 17, 2016 |
| Similar Recalls |