TruVision Health recalls Truv: 7-Day Experience Kit due to FDA-determined unsafe ingredients. Learn if you have the kit and what to do.
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
TruVision Health is recalling its Truvy 7-Day Experience Kit because it contains ingredients (DMHA and hordenine) that the FDA says are not safe for dietary use. This recall affects consumers who have purchased the kit and may pose health risks if used.
The kit contains DMHA and hordenine, which the FDA has identified as unsafe dietary ingredients. These substances are not approved for human consumption and could cause health issues if ingested.
Anyone who purchased the Truvy 7-Day Experience Kit from the manufacturer. People using the kit for dietary purposes are most at risk due to the unsafe ingredients.
Check for the product name 'Truvy 7-Day Experience Kit' and lot number 41404. The recall applies to kits sold by TruVision Health LLC.
Look for the lot number 41404 on the Truvy 7-Day Experience Kit to confirm if it is recalled.
No, the FDA has determined that the ingredients in this product are not safe for dietary use.
The recall does not specify a remedy, so check the product details to see if it is recalled and contact TruVision Health for further instructions.
Check for the lot number 41404 on the Truvy 7-Day Experience Kit.
We’ve drafted a message you can send TruVision Health to request your refund or repair — edit it as you like.
Subject: Recall F-0947-2023 — TruVision Health TruVision Health Hello, I own a TruVision Health that is covered by recall F-0947-2023 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.