Truvy Boost 30-Day Experience Kit
Recalling firm: TruVision Health LLC
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
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FDA code information
Lot 13993
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Full FDA record and distribution details
Original product description
Truvy Boost 30-Day Experience Kit
Recall details
- Recall number
- F-0948-2023
- Event ID
- 92173
- FDA status
- Ongoing
- Initiated
- Apr 27, 2023
- Reported
- May 31, 2023
- Classified
- May 25, 2023
- Quantity
- 22,125 packs
- Location
- Draper, UT, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Press Release
Where it was distributed
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
Data updated September 16, 2026. View official FDA data ↗
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