---
title: "TruBoost Drink - Ruby Rev — FDA record F-0951-2023 | Is It on Recall"
description: "The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients."
url: https://isitonrecall.com/recall/fda-food-f-0951-2023-truboost-drink-ruby-rev/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA food enforcement

# TruBoost Drink - Ruby Rev — FDA record F-0951-2023

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Apr 27, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: TruBoost Drink - Ruby Rev
- **Reason**: The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
- **Classification**: Class II
- **Recalling firm**: TruVision Health LLC
- **Quantity**: 4,650 packs
- **Agency-reported status**: Ongoing
- **Source record identifier**: F-0951-2023

[Open the official record](https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0951-2023%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Lot PM18821F1 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

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States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

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## Dates in the source

- **Report date**: May 31, 2023
- **Recall initiation date**: Apr 27, 2023
- **Center classification date**: May 25, 2023

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0951-2023%22)

## Related records

[Other food records](https://isitonrecall.com/category/other-food/) [TruVision Health LLC records](https://isitonrecall.com/brand/truvision-health-llc/)