---
title: "Monarch Platform REF MON-000005-01R, 100-240V- 50/60Hz 1440w — FDA record Z-0449-2024 | Is It on Recall"
description: "Their is the potential that software issues may result in flipped image of the virtual Bronchoscope view."
url: https://isitonrecall.com/recall/fda-device-z-0449-2024-monarch-platform-ref-mon-000005-01r-100-240v-50-60hz-1440w/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Monarch Platform REF MON-000005-01R, 100-240V- 50/60Hz 1440w — FDA record Z-0449-2024

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 Oct 18, 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**: Monarch Platform REF MON-000005-01R, 100-240V- 50/60Hz 1440w
- **Reason**: Their is the potential that software issues may result in flipped image of the virtual Bronchoscope view.
- **Classification**: Class II
- **Recalling firm**: AURIS HEALTH INC
- **Quantity**: 110 units In total
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0449-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0449-2024%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 | Software version 2.2.4 |

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

## Distribution

US Distribution: AK, AL, AZ, CA, CO, CT, DC, DE, FL, GA, IL, IN, KY, MA, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NY, OH, OR, PA, SC, SD, TN, TX, WI & WV.

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

- [Alaska](https://isitonrecall.com/state/alaska/)
- [Alabama](https://isitonrecall.com/state/alabama/)
- [Arizona](https://isitonrecall.com/state/arizona/)
- [California](https://isitonrecall.com/state/california/)
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- [District of Columbia](https://isitonrecall.com/state/district-of-columbia/)
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- [Georgia](https://isitonrecall.com/state/georgia/)
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- [North Dakota](https://isitonrecall.com/state/north-dakota/)
- [Nebraska](https://isitonrecall.com/state/nebraska/)
- [New Hampshire](https://isitonrecall.com/state/new-hampshire/)
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- [Oregon](https://isitonrecall.com/state/oregon/)
- [Pennsylvania](https://isitonrecall.com/state/pennsylvania/)
- [South Carolina](https://isitonrecall.com/state/south-carolina/)
- [South Dakota](https://isitonrecall.com/state/south-dakota/)
- [Tennessee](https://isitonrecall.com/state/tennessee/)
- [Texas](https://isitonrecall.com/state/texas/)
- [Wisconsin](https://isitonrecall.com/state/wisconsin/)
- [West Virginia](https://isitonrecall.com/state/west-virginia/)

## Dates in the source

- **Report date**: Dec 13, 2023
- **Recall initiation date**: Oct 18, 2023
- **Center classification date**: Dec 1, 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/device/enforcement.json?search=recall_number%3A%22Z-0449-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [AURIS HEALTH INC records](https://isitonrecall.com/brand/auris-health-inc/)