RegeneBlast — Class II food recall F-1824-2017
Terminated recall by VivaCeuticals, Inc. dba Regeneca Worldwide, reported 2017-04-12. The firm is recalling all herbal and dietary supplements because they were not manufactured in compliance with
| Recall number | F-1824-2017 |
|---|---|
| Product type | Food |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | VivaCeuticals, Inc. dba Regeneca Worldwide, Irvine, CA, United States |
| Recall initiated | 2017-03-09 |
| Classified | 2017-03-31 |
| Reported by FDA | 2017-04-12 |
| Terminated | 2017-08-08 |
| Reason classes | cgmp |
Product
RegeneBlast
Reason for recall
The firm is recalling all herbal and dietary supplements because they were not manufactured in compliance with the current Good Manufacturing Practice regulations for Dietary Supplements.
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-1824-2017. 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.