Truvy Boost Dietary Supplement Kit Recalled for Unapproved Ingredients
TruVision Health LLC is recalling Truvy Boost 30-Day Experience Kit (Lot 13993) because it contains DMHA and/or hordenine, which 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: Product contains DMHA and hordenine, which are risk-of-harm substances FDA has determined unacceptable for dietary supplements. While no illnesses have been reported in this recall, the ingredients pose inherent health risks.
Plain-English summary
TruVision Health LLC has recalled the Truvy Boost 30-Day Experience Kit due to the presence of DMHA and/or hordenine. The FDA has determined that these ingredients are not acceptable for use in dietary supplements.
The recalled product is the Truvy Boost 30-Day Experience Kit, Lot 13993. Approximately 22,125 packs were distributed in the United States and internationally to Australia, Canada, England, Germany, Ireland, and New Zealand.
Consumers who have purchased this product should discontinue use immediately. While no illnesses or injuries have been reported in association with this product, consumers with health concerns should consult their healthcare provider.
The recalled product
- Product
- Truvy Boost 30-Day Experience Kit
- Manufacturer
- TruVision Health LLC
- Category
- Drug — Dietary Supplement
- Affected units
- 22,125
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 13993
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.
See all 12 products in this recall →Related recalls
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