TruVision Health LLC recalls reFORM
- Recall date
- April 27, 2023
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- F-0942-2023
- FDA classification
- Class II
- Brand / firm
- TruVision Health LLC
- Sold / 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 Carol…
Why it was recalled
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
reFORM
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