truCONTROL
Reason The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
TruBoost 7 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
TruBoost 7 Day Experience Kit
Quantity: 14,510 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 13985
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-0949-2023 · 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.
TruControl 7 Day Trifold
Reason The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
reFORM
Reason The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
truControl W/Dynamine
Reason The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
TruWeight and Energy Gen 2+
Reason The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
TruWeight and Energy Gen 2+ Trifold
Reason The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
Truvy 30-Day Experience Kit
Reason The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
Truvy 7-Day Experience Kit
Reason The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
Truvy Boost 30-Day Experience Kit
Reason The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
TruBoost Drink Citrine Spark
Reason The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
TruBoost Drink Ruby Rev
Reason The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.