Venocell — Class II food recall F-1003-2017
Terminated recall by Sunset Natural Products Inc., reported 2017-01-04, distributed in FL, NV. Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until
| Recall number | F-1003-2017 |
|---|---|
| Product type | Food |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | FDA mandated |
| Recalling firm | Sunset Natural Products Inc., Miami, FL, United States |
| Recall initiated | 2015-10-13 |
| Classified | 2016-12-28 |
| Reported by FDA | 2017-01-04 |
| Terminated | 2017-04-10 |
| Distributed | FL, NV |
| Countries outside the US | DO |
| Quantity | 100,000 capsules |
| Reason classes | cgmp |
| Lot numbers | 04/17, 370414, 510414 |
Product
Venocell, bulk 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 manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/F-1003-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.