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TruVision Health LLC

12 recall records on file.

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12 recalls grouped by year

2023

12 records

Class IIOngoing05/31/2023Recall F-0940-2023

Product description

truCONTROL 60 Count

Reason for recall

The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.

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Event ID: 92173
Code info: Lot 13580
Product quantity: 73,450 packs
Distribution pattern: Alabama Alaska Arizona Arkansas California Colorado Connecticut Delaware Florida Georgia Hawaii Idaho Illinois Indiana Iowa Kansas Kentucky Louisiana Maine Maryland Massachusetts Michigan Minnesota Mississippi Missouri Montana Nebraska Nevada New Hampshire New Jersey New Mexico New York North Carolina North Dakota Ohio Oklahoma Oregon Pennsylvania Rhode Island South Carolina South Dakota Tennessee Texas Utah Vermont Virginia Washington West Virginia Wisconsin Wyoming and Australia, Canada, England, Germany, Ireland, New Zealand
Voluntary / mandated: Voluntary: Firm initiated
Initial firm notification: Press Release
Product type: Food
Recalling firm location: 172 E 14075 S, N/A, Draper, UT, United States
Recall initiation date: 04/27/2023
Center classification date: 05/25/2023

Class IIOngoing05/31/2023Recall F-0941-2023

Product description

TruControl 7 Day Trifold

Reason for recall

The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.

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Event ID: 92173
Code info: Lot WKW72353
Product quantity: Unknown
Distribution pattern: Alabama Alaska Arizona Arkansas California Colorado Connecticut Delaware Florida Georgia Hawaii Idaho Illinois Indiana Iowa Kansas Kentucky Louisiana Maine Maryland Massachusetts Michigan Minnesota Mississippi Missouri Montana Nebraska Nevada New Hampshire New Jersey New Mexico New York North Carolina North Dakota Ohio Oklahoma Oregon Pennsylvania Rhode Island South Carolina South Dakota Tennessee Texas Utah Vermont Virginia Washington West Virginia Wisconsin Wyoming and Australia, Canada, England, Germany, Ireland, New Zealand
Voluntary / mandated: Voluntary: Firm initiated
Initial firm notification: Press Release
Product type: Food
Recalling firm location: 172 E 14075 S, N/A, Draper, UT, United States
Recall initiation date: 04/27/2023
Center classification date: 05/25/2023

Class IIOngoing05/31/2023Recall F-0942-2023

Product description

reFORM

Reason for recall

The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.

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Event ID: 92173
Code info: Lot 34159
Product quantity: 2,535 packs
Distribution pattern: Alabama Alaska Arizona Arkansas California Colorado Connecticut Delaware Florida Georgia Hawaii Idaho Illinois Indiana Iowa Kansas Kentucky Louisiana Maine Maryland Massachusetts Michigan Minnesota Mississippi Missouri Montana Nebraska Nevada New Hampshire New Jersey New Mexico New York North Carolina North Dakota Ohio Oklahoma Oregon Pennsylvania Rhode Island South Carolina South Dakota Tennessee Texas Utah Vermont Virginia Washington West Virginia Wisconsin Wyoming and Australia, Canada, England, Germany, Ireland, New Zealand
Voluntary / mandated: Voluntary: Firm initiated
Initial firm notification: Press Release
Product type: Food
Recalling firm location: 172 E 14075 S, N/A, Draper, UT, United States
Recall initiation date: 04/27/2023
Center classification date: 05/25/2023

Class IIOngoing05/31/2023Recall F-0943-2023

Product description

truControl W/Dynamine 60 ct

Reason for recall

The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.

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Event ID: 92173
Code info: Lot WK65081
Product quantity: 31,353 packs
Distribution pattern: Alabama Alaska Arizona Arkansas California Colorado Connecticut Delaware Florida Georgia Hawaii Idaho Illinois Indiana Iowa Kansas Kentucky Louisiana Maine Maryland Massachusetts Michigan Minnesota Mississippi Missouri Montana Nebraska Nevada New Hampshire New Jersey New Mexico New York North Carolina North Dakota Ohio Oklahoma Oregon Pennsylvania Rhode Island South Carolina South Dakota Tennessee Texas Utah Vermont Virginia Washington West Virginia Wisconsin Wyoming and Australia, Canada, England, Germany, Ireland, New Zealand
Voluntary / mandated: Voluntary: Firm initiated
Initial firm notification: Press Release
Product type: Food
Recalling firm location: 172 E 14075 S, N/A, Draper, UT, United States
Recall initiation date: 04/27/2023
Center classification date: 05/25/2023

Class IIOngoing05/31/2023Recall F-0944-2023

Product description

TruWeight and Energy Gen 2+ 60 Count

Reason for recall

The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.

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Event ID: 92173
Code info: Lot WK71567
Product quantity: 4,182 packs
Distribution pattern: Alabama Alaska Arizona Arkansas California Colorado Connecticut Delaware Florida Georgia Hawaii Idaho Illinois Indiana Iowa Kansas Kentucky Louisiana Maine Maryland Massachusetts Michigan Minnesota Mississippi Missouri Montana Nebraska Nevada New Hampshire New Jersey New Mexico New York North Carolina North Dakota Ohio Oklahoma Oregon Pennsylvania Rhode Island South Carolina South Dakota Tennessee Texas Utah Vermont Virginia Washington West Virginia Wisconsin Wyoming and Australia, Canada, England, Germany, Ireland, New Zealand
Voluntary / mandated: Voluntary: Firm initiated
Initial firm notification: Press Release
Product type: Food
Recalling firm location: 172 E 14075 S, N/A, Draper, UT, United States
Recall initiation date: 04/27/2023
Center classification date: 05/25/2023

Class IIOngoing05/31/2023Recall F-0945-2023

Product description

TruWeight and Energy Gen 2+ Trifold

Reason for recall

The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.

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Event ID: 92173
Code info: Lot 25173
Product quantity: 6,793 packs
Distribution pattern: Alabama Alaska Arizona Arkansas California Colorado Connecticut Delaware Florida Georgia Hawaii Idaho Illinois Indiana Iowa Kansas Kentucky Louisiana Maine Maryland Massachusetts Michigan Minnesota Mississippi Missouri Montana Nebraska Nevada New Hampshire New Jersey New Mexico New York North Carolina North Dakota Ohio Oklahoma Oregon Pennsylvania Rhode Island South Carolina South Dakota Tennessee Texas Utah Vermont Virginia Washington West Virginia Wisconsin Wyoming and Australia, Canada, England, Germany, Ireland, New Zealand
Voluntary / mandated: Voluntary: Firm initiated
Initial firm notification: Press Release
Product type: Food
Recalling firm location: 172 E 14075 S, N/A, Draper, UT, United States
Recall initiation date: 04/27/2023
Center classification date: 05/25/2023

Class IIOngoing05/31/2023Recall F-0946-2023

Product description

Truvy 30-Day Experience Kit

Reason for recall

The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.

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Event ID: 92173
Code info: Lot 39643/42825
Product quantity: 9,693 packs
Distribution pattern: Alabama Alaska Arizona Arkansas California Colorado Connecticut Delaware Florida Georgia Hawaii Idaho Illinois Indiana Iowa Kansas Kentucky Louisiana Maine Maryland Massachusetts Michigan Minnesota Mississippi Missouri Montana Nebraska Nevada New Hampshire New Jersey New Mexico New York North Carolina North Dakota Ohio Oklahoma Oregon Pennsylvania Rhode Island South Carolina South Dakota Tennessee Texas Utah Vermont Virginia Washington West Virginia Wisconsin Wyoming and Australia, Canada, England, Germany, Ireland, New Zealand
Voluntary / mandated: Voluntary: Firm initiated
Initial firm notification: Press Release
Product type: Food
Recalling firm location: 172 E 14075 S, N/A, Draper, UT, United States
Recall initiation date: 04/27/2023
Center classification date: 05/25/2023

Class IIOngoing05/31/2023Recall F-0947-2023

Product description

Truvy 7-Day Experience Kit

Reason for recall

The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.

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Event ID: 92173
Code info: Lot 41404
Product quantity: 13,581 packs
Distribution pattern: Alabama Alaska Arizona Arkansas California Colorado Connecticut Delaware Florida Georgia Hawaii Idaho Illinois Indiana Iowa Kansas Kentucky Louisiana Maine Maryland Massachusetts Michigan Minnesota Mississippi Missouri Montana Nebraska Nevada New Hampshire New Jersey New Mexico New York North Carolina North Dakota Ohio Oklahoma Oregon Pennsylvania Rhode Island South Carolina South Dakota Tennessee Texas Utah Vermont Virginia Washington West Virginia Wisconsin Wyoming and Australia, Canada, England, Germany, Ireland, New Zealand
Voluntary / mandated: Voluntary: Firm initiated
Initial firm notification: Press Release
Product type: Food
Recalling firm location: 172 E 14075 S, N/A, Draper, UT, United States
Recall initiation date: 04/27/2023
Center classification date: 05/25/2023

Class IIOngoing05/31/2023Recall F-0948-2023

Product description

Truvy Boost 30-Day Experience Kit

Reason for recall

The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.

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Event ID: 92173
Code info: Lot 13993
Product quantity: 22,125 packs
Distribution pattern: Alabama Alaska Arizona Arkansas California Colorado Connecticut Delaware Florida Georgia Hawaii Idaho Illinois Indiana Iowa Kansas Kentucky Louisiana Maine Maryland Massachusetts Michigan Minnesota Mississippi Missouri Montana Nebraska Nevada New Hampshire New Jersey New Mexico New York North Carolina North Dakota Ohio Oklahoma Oregon Pennsylvania Rhode Island South Carolina South Dakota Tennessee Texas Utah Vermont Virginia Washington West Virginia Wisconsin Wyoming and Australia, Canada, England, Germany, Ireland, New Zealand
Voluntary / mandated: Voluntary: Firm initiated
Initial firm notification: Press Release
Product type: Food
Recalling firm location: 172 E 14075 S, N/A, Draper, UT, United States
Recall initiation date: 04/27/2023
Center classification date: 05/25/2023

Class IIOngoing05/31/2023Recall F-0949-2023

Product description

TruBoost 7 Day Experience Kit

Reason for recall

The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.

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Event ID: 92173
Code info: Lot 13985
Product quantity: 14,510 packs
Distribution pattern: Alabama Alaska Arizona Arkansas California Colorado Connecticut Delaware Florida Georgia Hawaii Idaho Illinois Indiana Iowa Kansas Kentucky Louisiana Maine Maryland Massachusetts Michigan Minnesota Mississippi Missouri Montana Nebraska Nevada New Hampshire New Jersey New Mexico New York North Carolina North Dakota Ohio Oklahoma Oregon Pennsylvania Rhode Island South Carolina South Dakota Tennessee Texas Utah Vermont Virginia Washington West Virginia Wisconsin Wyoming and Australia, Canada, England, Germany, Ireland, New Zealand
Voluntary / mandated: Voluntary: Firm initiated
Initial firm notification: Press Release
Product type: Food
Recalling firm location: 172 E 14075 S, N/A, Draper, UT, United States
Recall initiation date: 04/27/2023
Center classification date: 05/25/2023

Class IIOngoing05/31/2023Recall F-0950-2023

Product description

TruBoost Drink - Citrine Spark

Reason for recall

The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.

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Event ID: 92173
Code info: Lot PM17921F1
Product quantity: 1,789 packs
Distribution pattern: Alabama Alaska Arizona Arkansas California Colorado Connecticut Delaware Florida Georgia Hawaii Idaho Illinois Indiana Iowa Kansas Kentucky Louisiana Maine Maryland Massachusetts Michigan Minnesota Mississippi Missouri Montana Nebraska Nevada New Hampshire New Jersey New Mexico New York North Carolina North Dakota Ohio Oklahoma Oregon Pennsylvania Rhode Island South Carolina South Dakota Tennessee Texas Utah Vermont Virginia Washington West Virginia Wisconsin Wyoming and Australia, Canada, England, Germany, Ireland, New Zealand
Voluntary / mandated: Voluntary: Firm initiated
Initial firm notification: Press Release
Product type: Food
Recalling firm location: 172 E 14075 S, N/A, Draper, UT, United States
Recall initiation date: 04/27/2023
Center classification date: 05/25/2023

Class IIOngoing05/31/2023Recall F-0951-2023

Product description

TruBoost Drink - Ruby Rev

Reason for recall

The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.

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Event ID: 92173
Code info: Lot PM18821F1
Product quantity: 4,650 packs
Distribution pattern: Alabama Alaska Arizona Arkansas California Colorado Connecticut Delaware Florida Georgia Hawaii Idaho Illinois Indiana Iowa Kansas Kentucky Louisiana Maine Maryland Massachusetts Michigan Minnesota Mississippi Missouri Montana Nebraska Nevada New Hampshire New Jersey New Mexico New York North Carolina North Dakota Ohio Oklahoma Oregon Pennsylvania Rhode Island South Carolina South Dakota Tennessee Texas Utah Vermont Virginia Washington West Virginia Wisconsin Wyoming and Australia, Canada, England, Germany, Ireland, New Zealand
Voluntary / mandated: Voluntary: Firm initiated
Initial firm notification: Press Release
Product type: Food
Recalling firm location: 172 E 14075 S, N/A, Draper, UT, United States
Recall initiation date: 04/27/2023
Center classification date: 05/25/2023