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VivaCeuticals, Inc. dba Regeneca Worldwide

7 recall records on file.

2017

7 records

Class IITerminatedRecall F-1819-2017

Product description

RegeneSlim

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.

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Event ID
76634
Code info
Lot AAMXG
Product quantity
4000 units
Distribution pattern
US
Voluntary / mandated
Voluntary: Firm initiated
Initial firm notification
Press Release
Product type
Food
Recalling firm location
2 Park Plaza, Suite 1200, Irvine, CA, United States
Recall initiation date
03/09/2017
Center classification date
03/31/2017
Termination date
08/08/2017
Class IITerminatedRecall F-1820-2017

Product description

RegenErect

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.

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Event ID
76634
Code info
all lots
Product quantity
unknown
Distribution pattern
US
Voluntary / mandated
Voluntary: Firm initiated
Initial firm notification
Press Release
Product type
Food
Recalling firm location
2 Park Plaza, Suite 1200, Irvine, CA, United States
Recall initiation date
03/09/2017
Center classification date
03/31/2017
Termination date
08/08/2017
Class IITerminatedRecall F-1821-2017

Product description

RegeneArouse

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.

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Event ID
76634
Code info
all lots
Product quantity
unknown
Distribution pattern
US
Voluntary / mandated
Voluntary: Firm initiated
Initial firm notification
Press Release
Product type
Food
Recalling firm location
2 Park Plaza, Suite 1200, Irvine, CA, United States
Recall initiation date
03/09/2017
Center classification date
03/31/2017
Termination date
08/08/2017
Class IITerminatedRecall F-1822-2017

Product description

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.

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Event ID
76634
Code info
Lot AANAG
Product quantity
3000 units
Distribution pattern
US
Voluntary / mandated
Voluntary: Firm initiated
Initial firm notification
Press Release
Product type
Food
Recalling firm location
2 Park Plaza, Suite 1200, Irvine, CA, United States
Recall initiation date
03/09/2017
Center classification date
03/31/2017
Termination date
08/08/2017
Class IITerminatedRecall F-1823-2017

Product description

RegeneBoost

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.

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Event ID
76634
Code info
Lot ABQKH, ABQAB
Product quantity
1800 units
Distribution pattern
US
Voluntary / mandated
Voluntary: Firm initiated
Initial firm notification
Press Release
Product type
Food
Recalling firm location
2 Park Plaza, Suite 1200, Irvine, CA, United States
Recall initiation date
03/09/2017
Center classification date
03/31/2017
Termination date
08/08/2017
Class IITerminatedRecall F-1824-2017

Product description

RegeneBlast

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.

View full record
Event ID
76634
Code info
all lots
Product quantity
unknown
Distribution pattern
US
Voluntary / mandated
Voluntary: Firm initiated
Initial firm notification
Press Release
Product type
Food
Recalling firm location
2 Park Plaza, Suite 1200, Irvine, CA, United States
Recall initiation date
03/09/2017
Center classification date
03/31/2017
Termination date
08/08/2017
Class IITerminatedRecall 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.

View full record
Event ID
76634
Code info
LOT B1109329
Product quantity
300 units
Distribution pattern
US
Voluntary / mandated
Voluntary: Firm initiated
Initial firm notification
Press Release
Product type
Food
Recalling firm location
2 Park Plaza, Suite 1200, Irvine, CA, United States
Recall initiation date
03/09/2017
Center classification date
03/31/2017
Termination date
08/08/2017