FDAFDA · Food and drugs·Recall number F-1825-2017
RegeneFit
Published April 12, 2017 · Recall initiated: March 9, 2017
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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.
What to do
Voluntary: Firm initiated · Press Release
Recall details
- Manufacturer
- VivaCeuticals, Inc. dba Regeneca Worldwide
- Distributor
- US
- Lot
- LOT B1109329
- Risk classification
- Class II
- Area (FDA)
- food
- Country
- United States
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