The Recall Desk
ModerateFDA (Food)·F-0940-2023·Announced 2023-05-31

Dietary Supplement TruCONTROL Recalled Due to Unapproved Ingredients

TruVision Health's truCONTROL 60 Count dietary supplement is being recalled because it contains DMHA and/or hordenine, which the FDA has determined are not acceptable dietary ingredients.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: FDA Class II recall with no reported illnesses or injuries. The hazard is regulatory (unapproved ingredients) rather than an actual safety incident, making it a moderate-severity precautionary recall.

Plain-English summary

TruVision Health LLC is recalling truCONTROL 60 Count dietary supplements with lot number 13580. The product contains DMHA and/or hordenine, which the FDA has determined are not acceptable dietary ingredients.

73,450 packs have been distributed throughout the United States and internationally to Australia, Canada, England, Germany, Ireland, and New Zealand.

The recalled product

Product
truCONTROL 60 Count
Manufacturer
TruVision Health LLC
Category
Food — Dietary Supplement
Hazard
  • dmha
  • hordenine
  • unapproved-dietary-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 13580

Distribution

Distribution scope not specified by the agency.

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