The Recall Desk
HighFDA (Food)·F-0946-2023·Announced 2023-05-31

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.

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 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
  • unacceptable-ingredient

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

Distribution scope not specified by the agency.

Related recalls

Same category