TruVision Health LLC FDA recall records

The FDA has published 12 food recall enforcement records naming TruVision Health LLC between 2023 and 2023, covering 1 separate recall events. The firm is recorded in Utah. Data last updated 2 September 2026.

Records of 29,386
12
Share of all recalls
0%
Class I of 12
0
Reported between
2023 to 2023

What these records are

Every record on this page was published by the FDA in the openFDA food enforcement database. 12 records cover 1 recall events, because the agency opens one record per product code: a single recall of a product line with many codes appears here many times.

0 of these records are Class I, 12 Class II and 0 Class III. A recall count is not a safety score. Most FDA food recalls are initiated by the firm itself, and a recall is the firm removing product from the market, which is what a food safety plan is built to produce.

By year

Counts are by the date the FDA reported the enforcement action. That date runs behind the date a firm started a recall, so the most recent year is always partial.

Where the recalling firms are

The state is the location of the recalling firm, not where the product was sold. Distribution is recorded separately on each record.

Most recently reported

All 12 records.
ReportedProductFirmReasonClass
2023-05-31truControl W/Dynamine 60 ctTruVision Health LLCThe products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.Class II
2023-05-31TruWeight and Energy Gen 2+ 60 CountTruVision Health LLCThe products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.Class II
2023-05-31reFORMTruVision Health LLCThe products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.Class II
2023-05-31TruBoost Drink - Citrine SparkTruVision Health LLCThe products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.Class II
2023-05-31TruBoost Drink - Ruby RevTruVision Health LLCThe products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.Class II
2023-05-31Truvy 7-Day Experience KitTruVision Health LLCThe products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.Class II
2023-05-31Truvy 30-Day Experience KitTruVision Health LLCThe products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.Class II
2023-05-31TruControl 7 Day TrifoldTruVision Health LLCThe products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.Class II
2023-05-31TruWeight and Energy Gen 2+ TrifoldTruVision Health LLCThe products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.Class II
2023-05-31TruBoost 7 Day Experience KitTruVision Health LLCThe products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.Class II
2023-05-31Truvy Boost 30-Day Experience KitTruVision Health LLCThe products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.Class II
2023-05-31truCONTROL 60 CountTruVision Health LLCThe products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.Class II

Questions

How many FDA recalls has TruVision Health LLC had?
The FDA has published 12 food recall enforcement records naming TruVision Health LLC between 2023 and 2023. Those records cover 1 separate recall events: the agency opens one record per product code, so one recall of a product line appears as many records.
Does a high recall count mean a firm is unsafe?
Not on its own. Most FDA food recalls are initiated voluntarily by the firm, and a recall is the firm removing product from the market, which is what a working food safety plan is supposed to produce. Record counts also scale with the number of product codes a firm carries rather than with the number of things that went wrong.

All FDA food recall data

A recall is the end of an evidence trail that either existed or did not. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.

Early access

Recall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.