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Home / Food recalls / 2017

VivaCeuticals, Inc. dba Regeneca Worldwide

FDA recall F-1825-2017 · Class II · reported 2017-04-12 · Terminated

Product
RegeneFit
Reason
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.
Quantity
300 units
Distribution
US
Firm location
CA, United States
Initiated
Voluntary: Firm initiated
First notice
Press Release
Recall started
2017-03-09
Terminated
2017-08-08
Code info
LOT B1109329

Source: U.S. Food and Drug Administration, openFDA Food Enforcement database (openFDA Food Enforcement, imported 2026-09). The FDA does not validate openFDA data for completeness or accuracy. This is a record of an enforcement action, not safety advice.