The Recall Desk
HighFDA (Food)·F-0942-2023·Announced 2023-05-31

reFORM Dietary Supplement Recalled for Containing Unapproved Ingredients

TruVision Health LLC is recalling reFORM dietary supplement because it contains DMHA and/or hordenine, which the FDA has determined are not acceptable dietary ingredients.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: FDA Class II recall involving dietary ingredients the agency determined are not acceptable. No illnesses or injuries reported. This represents a regulatory risk-of-harm determination without demonstrated actual illness, fitting the Score 3 criterion of risk-of-harm products where injury has not yet been reported.

Plain-English summary

TruVision Health LLC is recalling reFORM, a dietary supplement product. The recall involves 2,535 packs with lot number 34159.

The product contains DMHA and/or hordenine, which the U.S. Food and Drug Administration (FDA) has determined are not acceptable dietary ingredients.

The product was distributed across all U.S. states and territories, as well as internationally to Australia, Canada, England, Germany, Ireland, and New Zealand. Consumers who have purchased this product should discontinue use and consult their healthcare provider with any questions or concerns.

The recalled product

Product
reFORM
Manufacturer
TruVision Health LLC
Category
Food — Dietary Supplement
Hazard
  • unapproved-ingredients

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 34159

Distribution

Distribution scope not specified by the agency.

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