Dietary supplement recalled for containing banned ingredients DMHA and hordenine
TruVision Health is recalling TruControl 7 Day Trifold dietary supplement (lot WKW72353) because it contains DMHA and hordenine, which the FDA determined are not acceptable dietary supplement 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: The product contains DMHA and hordenine, ingredients FDA has determined to be unacceptable for use in dietary supplements, representing a risk-of-harm product. No illnesses or injuries have been reported. This fits the rubric criterion for High severity: risk-of-harm products where injury has not yet been reported.
Plain-English summary
TruVision Health LLC is recalling the TruControl 7 Day Trifold dietary supplement because it contains DMHA and hordenine, which the FDA has determined are not acceptable dietary supplement ingredients.
The affected lot is WKW72353. The product was distributed nationwide in the United States and internationally to Australia, Canada, England, Germany, Ireland, and New Zealand.
The recalled product
- Product
- TruControl 7 Day Trifold
- Manufacturer
- TruVision Health LLC
- Category
- Food — Dietary Supplement
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 WKW72353
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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