TruBoost 7 Day Experience Kit
Recalling firm: TruVision Health LLC
Why it was recalled
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
The exact product
TruBoost 7 Day Experience Kit
Check the codes
Compare these FDA-provided codes, lot numbers or dates with the product you have.
Match the product, size and code together. A similar name alone does not identify your batch.
Original FDA code information
Lot 13985
Recall details
- Recall number
- F-0949-2023
- Event ID
- 92173
- FDA status
- Ongoing
- Initiated
- Apr 27, 2023
- Reported
- May 31, 2023
- Classified
- May 25, 2023
- Quantity
- 14,510 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 ↗
A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.