FDA recalls Truvy 30-Day Experience Kit due to unapproved dietary ingredients DMHA and hordenine. Consumers should stop using products containing these ingredients.
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
TruVision Health is recalling its Truvy 30-Day Experience Kit because it contains dietary ingredients (DMHA and hordenine) that the FDA has determined are not acceptable. This poses a health risk as these substances are not approved for use in food products.
The products contain DMHA and hordenine, which the FDA has identified as unapproved dietary ingredients. These substances are not safe for consumption and can pose health risks when ingested.
Anyone who purchased the Truvy 30-Day Experience Kit from the manufacturer. The risk is highest for individuals using the product for dietary purposes.
Check for the product name 'Truvy 30-Day Experience Kit' and lot numbers 39643 or 42825. The products were sold by TruVision Health LLC.
Immediately stop using the Truvy 30-Day Experience Kit if you have it.
The FDA has determined that the Truvy 30-Day Experience Kit contains unapproved dietary ingredients DMHA and hordenine.
Stop using the product immediately and contact TruVision Health for further instructions.
Yes, check for lot numbers 39643 or 42825 on the product.
We’ve drafted a message you can send TruVision Health to request your refund or repair — edit it as you like.
Subject: Recall F-0946-2023 — TruVision Health TruVision Health Hello, I own a TruVision Health that is covered by recall F-0946-2023 from TruVision Health. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
