FDAFDA · Food and drugs·Recall number F-0942-2023
reFORM
Published May 31, 2023 · Recall initiated: April 27, 2023
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
What to do
Voluntary: Firm initiated · Press Release
Recall details
- Manufacturer
- TruVision Health LLC
- Distributor
- 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
- Lot
- Lot 34159
- Risk classification
- Class II
- Area (FDA)
- food
- Country
- United States
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