PlainRecalls
FDA Food Moderate Class II Terminated

RegeneFit

Reported: April 12, 2017 Initiated: March 9, 2017 #F-1825-2017

Product Description

RegeneFit

Reason for Recall

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.

Details

Units Affected
300 units
Distribution
US
Location
Irvine, CA

Frequently Asked Questions

What product was recalled?
RegeneFit. Recalled by VivaCeuticals, Inc. dba Regeneca Worldwide. Units affected: 300 units.
Why was this product 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.
Which agency issued this recall?
This recall was issued by the FDA Food on April 12, 2017. Severity: Moderate. Recall number: F-1825-2017.