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FDA source record Class II Ongoing

TruBoost Drink - Ruby Rev

Recall Date: 2023-04-27 Recalling Firm: TruVision Health LLC Record Ref: F-0951-2023

FINDARECALL QUICK READ

What this record tells you

This FDA record concerns TruBoost Drink - Ruby Rev and names TruVision Health LLC as the recalling firm. Use the source fields below to narrow the match, then verify the exact item and current remedy on the issuing-agency page.

  • Firm: TruVision Health LLC
  • Classification: Class II
  • Status: Ongoing
  • Recall date: 2023-04-27
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Product Description & Identification

TruBoost Drink - Ruby Rev

Reason for Recall / Hazard Identified

The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.

How to Check Whether Your Product Matches

A matching product name or photograph is not enough by itself. Compare every identifier available on your item or packaging with the official notice.

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  2. Compare package size, color, flavor, model, style, or configuration when listed.
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  5. Open the official FDA source below and follow its current instructions.

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Consumer Action Recorded in the Source

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Distribution & Affected States

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Verify With the Issuing Agency

This record was last updated in our index on 2026-08-09 21:59:13 UTC. Because recall enforcement statuses and instructions evolve, always verify details directly with the issuing government agency.

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Record Transparency

Issuing agency
FDA
Source ID
F-0951-2023
Indexed update
2026-08-09 21:59:13 UTC
Official source
Open issuing-agency record