FDA Food recall F-0993-2017
Abte, bulk capsules
- FDA Food
- Class II
- terminated
- Published 2017-01-04
On 2017-01-04 the FDA classified a Class II recall of Abte, bulk 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-0993-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-10-13 |
| Published | 2017-01-04 |
| Last updated | 2026-09-13 11:49 UTC |
| Company | Sunset Natural Products |
| Distribution | FL, NV |
Product
Abte, bulk 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 manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.
Identifiers
| code_info | As persuant to the Consent Decree, the firm agreed to "recall and destroy, under FDA's supervision, in accordance with…As persuant to the Consent Decree, the firm agreed to "recall and destroy, under FDA's supervision, in accordance with the procedures provided in paragraph 6, ALL dietary supplements that were manufactured, prepared, processed, packed, labeled, held and/or distributed between April 2, 2014 and the date of entry of this Decree." The Decree was entered on September 25, 2015. Known lot and expiration date: Lot # 040714 Exp. Date 07/17 |
|---|
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-0993-2017%22
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