FDA recall record
TruBoost Drink - Ruby Rev
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
TruBoost Drink - Ruby Rev
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.
TruBoost Drink - Ruby Rev
Code information listed by FDA
Lot PM18821F1
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: 4,650 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.