MODERATE RISK
Terminated
F-1821-2017
RegeneArouse
Recalled by VivaCeuticals, Inc. dba Regeneca Worldwide
Classification
Class II — Products that might cause a temporary health problem, or pose only a slight threat of a serious nature.
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.
Product Details
Product Quantity
unknown
Product Type
Food
Code Info
all lots
Voluntary/Mandated
Voluntary: Firm initiated
Distribution & Geography
Distribution Pattern
US
Company Location
Irvine, CA, 92614-2562
Timeline
Report Date
04/12/2017
Recall Initiated
03/09/2017
Classification Date
03/31/2017
Termination Date
08/08/2017
Source: U.S. Food & Drug Administration (FDA) — FDA Recalls
Last updated: July 14, 2026
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