Recalls / Class II
Class IIF-0947-2023
Product
Truvy 7-Day Experience Kit
- Type
- Food
- Affected lot / code info
- Lot 41404
- Quantity
- 13,581 packs
Why it was recalled
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
Recalling firm
- Firm
- TruVision Health LLC
- Notification channel
- Press Release
- Type
- Voluntary: Firm initiated
- Address
- 172 E 14075 S, N/A, Draper, Utah 84020-5725
Distribution
- Distribution pattern
- 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
Timeline
- Recall initiated
- 2023-04-27
- FDA classified
- 2023-05-25
- Posted by FDA
- 2023-05-31
- Status
- Ongoing
Source: openFDA Food Enforcement endpoint. Recall record F-0947-2023. The FDA issues recall classifications as health-hazard assessments, not legal findings.