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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.