TruBoost Drink Ruby Rev recalled for unapproved dietary ingredients
TruVision Health LLC is recalling TruBoost Drink - Ruby Rev because it contains DMHA and/or hordenine, which the FDA has determined are not acceptable dietary ingredients.
The agency’s classification
FDA (Food): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 3/5 (High).
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: This is an FDA Class II recall involving unapproved dietary ingredients (DMHA and hordenine). Although no illnesses or injuries are reported, these stimulant ingredients pose a risk of adverse health effects and have been determined by FDA to be unacceptable in dietary supplements.
Plain-English summary
TruVision Health LLC is recalling TruBoost Drink - Ruby Rev. The product contains DMHA and/or hordenine, which the FDA has determined are not acceptable dietary ingredients.
Approximately 4,650 packs of the product with lot code PM18821F1 are affected. The recall includes distributions to all U.S. states and international locations including Australia, Canada, England, Germany, Ireland, and New Zealand.
The recalled product
- Product
- TruBoost Drink - Ruby Rev
- Manufacturer
- TruVision Health LLC
- Category
- Food — Dietary Supplement
- Affected units
- 4,650
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Lot PM18821F1
Distribution
Part of a larger recall action
This product is one of 12 recalled by TruVision Health LLC under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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