RegeneFit
Recalling firm: VivaCeuticals, Inc. dba Regeneca Worldwide
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.
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ProductRegeneFit
FDA code information
LOT B1109329
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Full FDA record and distribution details
Original product description
RegeneFit
Recall details
- Recall number
- F-1825-2017
- Event ID
- 76634
- FDA status
- Terminated
- Initiated
- Mar 9, 2017
- Reported
- Apr 12, 2017
- Classified
- Mar 31, 2017
- Terminated
- Aug 8, 2017
- Quantity
- 300 units
- Location
- Irvine, CA, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Press Release
Where it was distributed
US
FDA source record · F-1825-2017
Data updated September 16, 2026. View official FDA data ↗
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