FDA recalls TruWeight and Energy Gen 2+ 60-count products due to containing unapproved dietary ingredients DMHA and hordenine. 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 has recalled two dietary products, TruWeight and Energy Gen 2+, because they contain ingredients (DMHA and hordenine) that the FDA says are not approved for use in food. This means these products are unsafe to consume as they may pose health risks.
The products contain DMHA and hordenine, which the FDA has determined are not acceptable dietary ingredients. This means they could cause health issues when consumed, though the exact risk level isn't specified in the recall.
Anyone who purchased TruWeight or Energy Gen 2+ 60-count products with lot number WK71567 from TruVision Health. People using these products for weight management or energy are most at risk.
Check for the product name (TruWeight or Energy Gen 2+) and lot number WK71567 on the packaging. These products were sold by TruVision Health.
Look for the product name and lot number WK71567 on the packaging to confirm if it's affected.
The FDA has determined that DMHA and hordenine are not acceptable dietary ingredients in these products.
Check the product name and lot number WK71567 to see if it's affected. If so, stop using it.
The FDA has identified these ingredients as unsafe, but the specific health risks aren't detailed in the recall notice.
We’ve drafted a message you can send TruVision Health to request your refund or repair — edit it as you like.
Subject: Recall F-0944-2023 — TruVision Health TruVision Health Hello, I own a TruVision Health that is covered by recall F-0944-2023 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.
