Home / TruVision Health LLC / F-0946-2023
Class IIOngoing
TruVision Health LLC
Recall #F-0946-2023 · Initiated 2023-04-27
Plain-language summary
by FoodRecallsDB.infoWhat happened
TruVision Health LLC is recalling their Truvy 30-Day Experience Kit because it contains ingredients called DMHA and hordenine that the FDA says should not be in dietary supplements. About 9,700 packs were distributed across the U.S. and several other countries.
Who is at risk
Anyone who purchased and used this product should be aware of the recall, as these ingredients may pose health risks.
What to do
Stop using the product immediately if you have it. Contact TruVision Health LLC or check the FDA website for information about returning the product or getting a refund. If you experience any health problems after using this product, contact your doctor or poison control.
Product
Truvy 30-Day Experience Kit
Reason for recall
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
Quantity affected
9,693 packs
Distribution
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
Lot / code info
Lot 39643/42825
Voluntary / mandated
Voluntary: Firm initiated
Initial notification
Press Release
Recalling firm
TruVision Health LLC
172 E 14075 S
Draper, UT 84020-5725
United States
Recall classification
Remote probability of serious adverse health consequences, or temporary reversible consequences.