---
title: "Brand Name: Rover Product Name: Mobile X-ray System Model/Catalog Number:MXU-... — FDA record Z-1670-2025 | Is It on Recall"
description: "Potential for internal fastening mechanism within generator of mobile x-Ray to fail."
url: https://isitonrecall.com/recall/fda-device-z-1670-2025-brand-name-rover-product-name-mobile-x-ray-system-model-catalog-number-mxu-rv35-product-description/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Brand Name: Rover Product Name: Mobile X-ray System Model/Catalog Number:MXU-RV35 Product Description: Rover Mobile X... — FDA record Z-1670-2025

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 Apr 4, 2025. 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**: Brand Name: Rover Product Name: Mobile X-ray System Model/Catalog Number:MXU-RV35 Product Description: Rover Mobile X-rays System ("Rover") is a mobile imaging system that incorporates a self-contained X-ray generator, imaging display and software for acquiring medical diagnostic images outside a standard X-ray room. It is designed specifically for Digital Radiography (DR) with vendor-supported detectors. The Rover is designed to perform radiographic X-ray examinations for disease/injury detection, diagnosis, medical and surgical treatment planning, and therapy monitoring, where patient condition contraindicates transport to a fixed X-ray unit The Rover can be used on pediatric and adult patients, in all patient treatment areas Component: N/A
- **Reason**: Potential for internal fastening mechanism within generator of mobile x-Ray to fail.
- **Classification**: Class II
- **Recalling firm**: Micro-X Ltd.
- **Quantity**: 5 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1670-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1670-2025%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 | Serial Number/UDI-DI - 349 (01)09357123000037(11)230209(21)00349 348 (01)09357123000037(11)230123(21)00348 350 (01)09357123000037(11)230328(21)00350. 351 (01)09357123000037(11)230413(21)00351 361 (01)09357123000037(11)230503(21)00361 |

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

## Distribution

US: NJ, WA, Puerto Rico OUS: None

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

- [New Jersey](https://isitonrecall.com/state/new-jersey/)
- [Washington](https://isitonrecall.com/state/washington/)

## Dates in the source

- **Report date**: Apr 30, 2025
- **Recall initiation date**: Apr 4, 2025
- **Center classification date**: Apr 24, 2025

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-1670-2025%22)

## Related records

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