Truvy 30-Day Experience Kit Recalled for Unacceptable Dietary Ingredients
TruVision Health LLC is recalling Truvy 30-Day Experience Kit 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: This is a Class II recall involving ingredients the FDA determined are not acceptable, constituting a risk-of-harm product. No illnesses or injuries are reported in the source, aligning with severity Score 3 per the FDA rubric.
Plain-English summary
TruVision Health LLC is recalling approximately 9,693 packs of Truvy 30-Day Experience Kit because the product contains DMHA and/or hordenine. The FDA has determined that these ingredients are not acceptable for use in dietary supplements.
The affected product was distributed in all 50 U.S. states as well as Australia, Canada, England, Germany, Ireland, and New Zealand. The recalled product includes lot numbers 39643/42825.
Consumers who have purchased this product should stop using it. Those with questions or concerns should contact TruVision Health LLC or consult their healthcare provider.
The recalled product
- Product
- Truvy 30-Day Experience Kit
- Manufacturer
- TruVision Health LLC
- Category
- Food — Dietary Supplement
- Hazard
- Affected units
- 9,693
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 39643/42825
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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