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
Affected units
73,450

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

Part of a larger recall action

This product is one of 12 recalled by TruVision Health LLC under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 12 products in this recall →