Terminated
Class II
VivaCeuticals, Inc. dba Regeneca Worldwide
Recall F-1825-2017 · Irvine, CA
Product
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.
Distribution
US
Quantity affected
300 units
Recall type
Voluntary: Firm initiated
Lot / code info
LOT B1109329
Timeline
9 Mar 2017 initiated
→
31 Mar 2017 classified
→
12 Apr 2017 reported
→
8 Aug 2017 terminated
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