TruBoost 7 Day Experience Kit dietary supplement recalled for prohibited ingredients
TruVision Health LLC recalls TruBoost 7 Day Experience Kit due to the presence of DMHA and/or hordenine, which the FDA determined are not acceptable dietary ingredients.
What this means for you
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 product contains DMHA and hordenine, which are prohibited dietary ingredients that FDA has determined are not acceptable. While no illnesses or injuries have been reported, these are known stimulant compounds with recognized safety concerns, fitting the profile of risk-of-harm products where injury has not yet been reported.
Plain-English summary
TruVision Health LLC is recalling the TruBoost 7 Day Experience Kit, a dietary supplement product, because it contains DMHA and/or hordenine, which the FDA has determined are not acceptable dietary ingredients.
The recalled product, lot 13985, was distributed nationwide in all U.S. states as well as in Australia, Canada, England, Germany, Ireland, and New Zealand. A total of 14,510 packs are affected by this recall.
The recalled product
- Product
- TruBoost 7 Day Experience Kit
- Manufacturer
- TruVision Health LLC
- Category
- Food — Dietary Supplement
- Affected units
- 14,510
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 13985
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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