TruVision Health recalls reFORM products containing unapproved dietary ingredients DMHA and hordenine, which FDA deems unsafe. Consumers should check lot numbers for affected items.
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
TruVision Health is recalling reFORM products because they contain DMHA and hordenine, substances the FDA has determined are not acceptable dietary ingredients. This recall is necessary to prevent potential health risks from consuming these unapproved ingredients.
The products contain DMHA and hordenine, which the FDA has identified as substances that are not approved for use in dietary ingredients. Consuming these ingredients could pose health risks, though the specific risks are not detailed in the recall notice.
Anyone who purchased reFORM products with lot number 34159. The risk is low as the products are food items and the hazard involves unapproved ingredients rather than immediate physical danger.
Check for the lot number 34159 on the reFORM product packaging. The affected products are labeled as reFORM with this specific lot number.
Look for the lot number 34159 on the reFORM product packaging to identify affected items.
The FDA has determined that DMHA and hordenine are not acceptable dietary ingredients, so TruVision Health is recalling reFORM products with lot number 34159.
Check the lot number on the product packaging. If it is 34159, you should stop using it and contact TruVision Health for further instructions.
The recall states that the products contain unapproved dietary ingredients, but does not mention any risk of serious injury or physical harm. The hazard level is low risk.
We’ve drafted a message you can send TruVision Health to request your refund or repair — edit it as you like.
Subject: Recall F-0942-2023 — TruVision Health TruVision Health Hello, I own a TruVision Health that is covered by recall F-0942-2023 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.
