Truvy 30-Day Experience Kit
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
What to do
- 1Do not eat it.
- 2Return or discard the product.
- 3Watch for symptoms if you already had some.
Recall details
- Firm
- TruVision Health LLC
- Status
- Ongoing
- Reported
- May 31, 2023
- Started
- Apr 27, 2023
- Where sold
- 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
- Quantity
- 9,693 packs
- FDA number
- F-0946-2023
Lots, UPC, dates
Lot 39643/42825
FDA wording
Truvy 30-Day Experience Kit
Source: FDA report. This is not medical advice. Compare your package codes before you act.