FDA recall F-1820-2017
VivaCeuticals, Inc. dba Regeneca Worldwide · Class II · food
Product
RegenErect
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
- 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
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=F-1820-2017