The Recall Desk
HighFDA (Food)·F-0949-2023·Announced 2023-05-31

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
Hazard
  • dmha
  • hordenine

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

Distribution scope not specified by the agency.

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