FDA Food recall F-0537-2016
Argindione, sold as bulk of 50,000 capsules
- FDA Food
- Class II
- terminated
- Published 2016-02-24
On 2016-02-24 the FDA classified a Class II recall of Argindione, sold as bulk of 50,000 capsules by Sunset Natural Products, citing 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….
Read the official FDA Food notice
| Agency | FDA Food |
|---|---|
| Recall number | F-0537-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-10-05 |
| Published | 2016-02-24 |
| Last updated | 2026-09-13 11:49 UTC |
| Company | Sunset Natural Products |
| Distribution | FL, NV |
Product
Argindione, sold as 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.
Identifiers
| code_info | Lot # 480514 Exp. Date 05/17 and Lot # 320614 Exp. Date 06/17 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:49 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0537-2016%22
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