---
title: "MICRO-X Rover Mobile X-ray System, # MXU-RV35 — FDA record Z-0580-2025 | Is It on Recall"
description: "Mobile x-ray system receiving/storage(operation) requirements to be followed: Temp:14 to 131(50 to 86) degrees F, RH:10% to 86%(30% to 60%) allow condensation d"
url: https://isitonrecall.com/recall/fda-device-z-0580-2025-micro-x-rover-mobile-x-ray-system-mxu-rv35/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# MICRO-X Rover Mobile X-ray System, # MXU-RV35 — FDA record Z-0580-2025

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 22, 2024. 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**: MICRO-X Rover Mobile X-ray System, # MXU-RV35
- **Reason**: Mobile x-ray system receiving/storage(operation) requirements to be followed: Temp:14 to 131(50 to 86) degrees F, RH:10% to 86%(30% to 60%) allow condensation dry time, Atmospheric Pressure:50kPa to 106 kPa(70kPa to 106kPa), Altitude:-102ft to 12,000 ft, (Maximum Gradient:9 degrees Fahrenheit), which mitigate risk of capacitor malfunction, unpredictable behavior, overheating, unintended start-up.
- **Classification**: Class II
- **Recalling firm**: Micro-X Ltd.
- **Quantity**: 6
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0580-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0580-2025%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 | UDI-DI: 9357123000037, Serial Numbers: 348, 349, 361, 351, 365, 391 |

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

## Distribution

US: TX, PR, MD, CA

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

- [California](https://isitonrecall.com/state/california/)
- [Maryland](https://isitonrecall.com/state/maryland/)
- [Texas](https://isitonrecall.com/state/texas/)

## Dates in the source

- **Report date**: Dec 4, 2024
- **Recall initiation date**: Oct 22, 2024
- **Center classification date**: Nov 27, 2024

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-0580-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Micro-X Ltd. records](https://isitonrecall.com/brand/micro-x-ltd/)