FDA Food recall F-0617-2016
Hepasil, sold in bulk of 500,000 capsules
- FDA Food
- Class II
- terminated
- Published 2016-02-24
On 2016-02-24 the FDA classified a Class II recall of Hepasil, sold in bulk of 500,000 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-0617-2016 |
| 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
Hepasil, sold in bulk of 500,000 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 # 080315 Exp. Date 03/18 |
|---|
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-0617-2016%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.