Terminated
Class II
VivaCeuticals, Inc. dba Regeneca Worldwide
Recall F-1822-2017 · Irvine, CA
Product
RegeneBlend
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
3000 units
Recall type
Voluntary: Firm initiated
Lot / code info
Lot AANAG
Timeline
9 Mar 2017 initiated
→
31 Mar 2017 classified
→
12 Apr 2017 reported
→
8 Aug 2017 terminated
Sourced directly from the FDA’s openFDA enforcement database. This information is for educational purposes only and does not constitute health or legal advice. FoodRecallFinder.com is not affiliated with or endorsed by the U.S. Food and Drug Administration.