Recalls / Class II
Class IIF-1821-2017
Product
RegeneArouse
- Type
- Food
- Affected lot / code info
- all lots
- Quantity
- unknown
Why it was recalled
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.
Recalling firm
- Firm
- VivaCeuticals, Inc. dba Regeneca Worldwide
- Notification channel
- Press Release
- Type
- Voluntary: Firm initiated
- Address
- 2 Park Plaza, Suite 1200, Irvine, California 92614-2562
Distribution
- Distribution pattern
- US
Timeline
- Recall initiated
- 2017-03-09
- FDA classified
- 2017-03-31
- Posted by FDA
- 2017-04-12
- Terminated
- 2017-08-08
- Status
- Terminated
Source: openFDA Food Enforcement endpoint. Recall record F-1821-2017. The FDA issues recall classifications as health-hazard assessments, not legal findings.