Food Recall Check
Class II · Moderate risk Ongoing Initiated Apr 27, 2023 (3 years ago)

Truvy 30-Day Experience Kit recall

Recalled by TruVision Health LLC · Draper, UT, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

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

See the recall's own reason text for the specifics. All other reasons recalls.

What was recalled

Truvy 30-Day Experience Kit

Quantity: 9,693 packs

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Lot 39643/42825

Where it was sold

Alaska Alabama Arkansas Arizona California Colorado Connecticut Delaware Florida Georgia Hawaii Iowa Idaho Illinois Indiana Kansas Kentucky Louisiana Massachusetts Maryland Maine Michigan Minnesota Missouri Mississippi Montana North Carolina North Dakota Nebraska New Hampshire New Jersey New Mexico Nevada New York Ohio Oklahoma Oregon Pennsylvania Rhode Island South Carolina South Dakota Tennessee Texas Utah Virginia Vermont Washington Wisconsin West Virginia Wyoming

FDA's distribution note: 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

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away.

Recalling firm
TruVision Health LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Apr 27, 2023
In FDA report of
May 31, 2023
FDA recall number
F-0946-2023 · event 92173
Official record
FDA enforcement report search

Also recalled with it (11 more products)

FDA files each product of one recall action separately; these share the same FDA event.

Class II · Moderate risk Ongoing Other

truCONTROL

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

TruVision Health LLC 50 states F-0940-2023
Class II · Moderate risk Ongoing Other

TruControl 7 Day Trifold

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

TruVision Health LLC 50 states F-0941-2023
Class II · Moderate risk Ongoing Other

reFORM

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

TruVision Health LLC 50 states F-0942-2023
Class II · Moderate risk Ongoing Other

truControl W/Dynamine

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

TruVision Health LLC 50 states F-0943-2023
Class II · Moderate risk Ongoing Other

TruWeight and Energy Gen 2+

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

TruVision Health LLC 50 states F-0944-2023
Class II · Moderate risk Ongoing Other

TruWeight and Energy Gen 2+ Trifold

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

TruVision Health LLC 50 states F-0945-2023
Class II · Moderate risk Ongoing Other

Truvy 7-Day Experience Kit

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

TruVision Health LLC 50 states F-0947-2023
Class II · Moderate risk Ongoing Other

Truvy Boost 30-Day Experience Kit

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

TruVision Health LLC 50 states F-0948-2023
Class II · Moderate risk Ongoing Other

TruBoost 7 Day Experience Kit

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

TruVision Health LLC 50 states F-0949-2023
Class II · Moderate risk Ongoing Other

TruBoost Drink Citrine Spark

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

TruVision Health LLC 50 states F-0950-2023
Class II · Moderate risk Ongoing Other

TruBoost Drink Ruby Rev

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

TruVision Health LLC 50 states F-0951-2023