WHY THIS PRODUCT IS LISTED
Other / see reason
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
Product description & recall reason
The recall record describes “Truvy Boost 30-Day Experience Kit”; the source reports: “The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.”
Based on the official recall record; packaging and sales claims have not been verified. Verify with the official source ↗
Identify the product
- Product description
- Truvy Boost 30-Day Experience Kit
- Brand
- Not supplied by this source
- Lot, batch, UPC & other codes
- Lot 13993
- Quantity
- 22,125 packs
Where it came from & where it went
- Recalling firm
- TruVision Health LLC
- Recalling firm address
- 172 E 14075 S; N/A; Draper; UT; 84020-5725; United States
- Product production / origin location
- Not supplied by this source
- Distribution — source wording
- 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
States identified in the source
Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin, West Virginia, Wyoming