FDA recall record
Truvy Boost 30-Day Experience Kit
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
Product described in an FDA recall
Truvy Boost 30-Day Experience Kit
Reason
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
Truvy Boost 30-Day Experience Kit
Code information listed by FDA
Lot 13993
Distribution and firm information
Recalling firm listed by FDA: TruVision Health LLC
Firm location listed by FDA: Draper, UT, United States
Distribution reported by FDA: 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
Product quantity listed by FDA: 22,125 packs
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.