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TruVision Health LLC
FDA recall F-0946-2023 · Class II · reported 2023-05-31 · Ongoing
- Product
- Truvy 30-Day Experience Kit
- Reason
- The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
- Quantity
- 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
- Firm location
- UT, United States
- Initiated
- Voluntary: Firm initiated
- First notice
- Press Release
- Recall started
- 2023-04-27
- Code info
- Lot 39643/42825
Source: U.S. Food and Drug Administration, openFDA Food Enforcement database (openFDA Food Enforcement, imported 2026-09). The FDA does not validate openFDA data for completeness or accuracy. This is a record of an enforcement action, not safety advice.