MODERATE RISK
Ongoing
F-0951-2023
TruBoost Drink - Ruby Rev
Recalled by TruVision Health LLC
Classification
Class II — Products that might cause a temporary health problem, or pose only a slight threat of a serious nature.
Reason for Recall
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
Product Details
Product Quantity
4,650 packs
Product Type
Food
Code Info
Lot PM18821F1
Voluntary/Mandated
Voluntary: Firm initiated
Distribution & Geography
Distribution Pattern
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
Company Location
Draper, UT, 84020-5725
Timeline
Report Date
05/31/2023
Recall Initiated
04/27/2023
Classification Date
05/25/2023
Termination Date
N/A
Source: U.S. Food & Drug Administration (FDA) — FDA Recalls
Last updated: August 28, 2026
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