Skip to content
Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 92173

12 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
April 27, 2023
Product types
Food
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
TruVision Health LLC

Dossier provenance

Source snapshots represented here

  • openFDA Food Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

12 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

food · product 1 of 12

truCONTROL 60 Count

F-0940-2023
Recall number
F-0940-2023
Initiated
April 27, 2023
Classification
Class II
Status
Ongoing
Recalling firm
TruVision Health LLC
Quantity
73,450 packs

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

Lot 13580

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

food · product 2 of 12

TruControl 7 Day Trifold

F-0941-2023
Recall number
F-0941-2023
Initiated
April 27, 2023
Classification
Class II
Status
Ongoing
Recalling firm
TruVision Health LLC
Quantity
Unknown

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

Lot WKW72353

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

food · product 3 of 12

reFORM

F-0942-2023
Recall number
F-0942-2023
Initiated
April 27, 2023
Classification
Class II
Status
Ongoing
Recalling firm
TruVision Health LLC
Quantity
2,535 packs

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

Lot 34159

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

food · product 4 of 12

truControl W/Dynamine 60 ct

F-0943-2023
Recall number
F-0943-2023
Initiated
April 27, 2023
Classification
Class II
Status
Ongoing
Recalling firm
TruVision Health LLC
Quantity
31,353 packs

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

Lot WK65081

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

food · product 5 of 12

TruWeight and Energy Gen 2+ 60 Count

F-0944-2023
Recall number
F-0944-2023
Initiated
April 27, 2023
Classification
Class II
Status
Ongoing
Recalling firm
TruVision Health LLC
Quantity
4,182 packs

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

Lot WK71567

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

food · product 6 of 12

TruWeight and Energy Gen 2+ Trifold

F-0945-2023
Recall number
F-0945-2023
Initiated
April 27, 2023
Classification
Class II
Status
Ongoing
Recalling firm
TruVision Health LLC
Quantity
6,793 packs

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

Lot 25173

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

food · product 7 of 12

Truvy 30-Day Experience Kit

F-0946-2023
Recall number
F-0946-2023
Initiated
April 27, 2023
Classification
Class II
Status
Ongoing
Recalling firm
TruVision Health LLC
Quantity
9,693 packs

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

Lot 39643/42825

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

food · product 8 of 12

Truvy 7-Day Experience Kit

F-0947-2023
Recall number
F-0947-2023
Initiated
April 27, 2023
Classification
Class II
Status
Ongoing
Recalling firm
TruVision Health LLC
Quantity
13,581 packs

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

Lot 41404

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

food · product 9 of 12

Truvy Boost 30-Day Experience Kit

F-0948-2023
Recall number
F-0948-2023
Initiated
April 27, 2023
Classification
Class II
Status
Ongoing
Recalling firm
TruVision Health LLC
Quantity
22,125 packs

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

Lot 13993

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

food · product 10 of 12

TruBoost 7 Day Experience Kit

F-0949-2023
Recall number
F-0949-2023
Initiated
April 27, 2023
Classification
Class II
Status
Ongoing
Recalling firm
TruVision Health LLC
Quantity
14,510 packs

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

Lot 13985

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

food · product 11 of 12

TruBoost Drink - Citrine Spark

F-0950-2023
Recall number
F-0950-2023
Initiated
April 27, 2023
Classification
Class II
Status
Ongoing
Recalling firm
TruVision Health LLC
Quantity
1,789 packs

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

Lot PM17921F1

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

food · product 12 of 12

TruBoost Drink - Ruby Rev

F-0951-2023
Recall number
F-0951-2023
Initiated
April 27, 2023
Classification
Class II
Status
Ongoing
Recalling firm
TruVision Health LLC
Quantity
4,650 packs

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

Lot PM18821F1

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