# FDA recall F-1822-2017

> **VivaCeuticals, Inc. dba Regeneca Worldwide** · Class II · food recall initiated 2017-03-09.

## Product

RegeneBlend

## 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.

## Distribution

US

## Key facts

- **Recall number:** F-1822-2017
- **Recalling firm:** VivaCeuticals, Inc. dba Regeneca Worldwide
- **Classification:** Class II
- **Product type:** food
- **Status:** Terminated
- **Initiation date:** 2017-03-09
- **Report date:** 2017-04-12
- **Termination date:** 2017-08-08

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Irvine, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=F-1822-2017

## Citation

> AI Analytics. FDA recall F-1822-2017. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/F-1822-2017. Source: US FDA. Licensed CC0.

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