Key Takeaway
RegeneFit by VivaCeuticals, Inc. dba Regeneca Worldwide was recalled on March 9, 2017. The hazard: The firm is recalling all herbal and dietary supplements because they were not manufactured in compliance with the current Good Manufacturing Practice...
RegeneFit
Description
RegeneFit
Hazard / 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.
Class II: Product that may cause temporary or medically reversible health consequences.
Class II indicates the product may cause temporary or medically reversible health effects. The probability of serious harm is considered remote.
Company Information
VivaCeuticals, Inc. dba Regeneca Worldwide
Irvine, CA, United States
View all 7 recalls by VivaCeuticals, Inc. dba Regeneca Worldwide →Distribution
US
Related Recalls
Frequently Asked Questions
Is this recall still active?
Check the status badge at the top of this page. "Ongoing" means the recall is still active and you should follow the remedy instructions. "Completed" or "Terminated" means the recall process has concluded, though the safety issue remains relevant for any unrepaired products.
How do I check if my product is affected?
Compare the model number, lot code, serial number, or date range listed in the recall notice with the information on your product's label or packaging. For vehicles, check your VIN at NHTSA.gov/Recalls.
What remedy is available for this recall?
Check the remedy section above or contact the manufacturer directly for current remedy options.
Where can I find the original recall notice?
This recall was issued by FDA Food. Visit the agency's official website for the original notice.