Recall Register

Food, drugs, devices › Micro-X Ltd.

Device recall: MICRO-X Rover Mobile X-ray System, # MXU-RV19

FDA enforcement event 95593 · Class II · initiated 23 Oct 2024 · status Ongoing

DeviceVoluntary: Firm initiated1 product record

Micro-X Ltd. (Tonsley) initiated this device recall on 23 Oct 2024; FDA lists 1 product record under event 95593, classified Class II.

FDA defines Class II as a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote. 87% of the 970 device enforcement events initiated in 2024 carry the same class.

Status: Ongoing. Initiation: voluntary: firm initiated. Micro-X Ltd. has 8 enforcement events on this register, with a median of 1 product record per event.

Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.

Recalling firm

Micro-X Ltd., Tonsley, Australia.

Reason for recall

"During internal testing it was found that if the system is Ready to expose and the hand switch is then dropped into the stowage unit such that it lands on the prep/expose switch, the prep switch can be activated for a very short time such that the orange ring of death is displayed in the tube cooling area of the screen. The system then becomes unresponsive to kV/mAs changes, prep/expose presses.…"

Distribution

"US Nationwide Distribution: TX, CA, OH, ID, WA, AZ"

Product records

Recall numberProductQuantityClassStatusReport date
Z-0666-2025MICRO-X Rover Mobile X-ray System, # MXU-RV1923Class IIOngoing18 Dec 2024

Context

87%of 2024 device events are Class II970 events that year
1product record in this eventfirm median: 1
8events on this register for the firm

Other enforcement events for Micro-X Ltd.

InitiatedProduct (first record)TypeClassRecords
27 Mar 2026Rover Mobile X-ray System Model/Catalog Number: MXU-RV35 and MXU-RV71DeviceClass II1
4 Apr 2025Brand Name: Rover Product Name: Mobile X-ray System Model/Catalog Number: MXU-RV71, MXU-RV35 Product Description: Rover DeviceClass II2
28 Mar 2025Brand Name: Rover Product Name: Mobile X-ray System Model/Catalog Number: MXU-RV71 Product Description: Rover Mobile X-rDeviceClass II2
22 Oct 2024MICRO-X Rover Mobile X-ray System, # MXU-RV35DeviceClass II1
28 Nov 2023MICRO-X Rover Mobile X-ray System, # MXU-RV35; MICRO-X Rover Mobile X-ray System, # MXU-RV71DeviceClass II1
31 May 2023MICRO-X Rover Mobile X-ray System, # MXU-RV35DeviceClass II1
31 Aug 2022MICRO-X ROVER MOBILE X-RAY SYSTEM, MXU-RV19DeviceClass II1

All 8 events for Micro-X Ltd.

Questions and answers

Why was this device recalled?

FDA's record gives the reason for recall as: "During internal testing it was found that if the system is Ready to expose and the hand switch is then dropped into the stowage unit such that it lands on the prep/expose switch, the prep switch can be activated for a very short time such that the orange ring of death is displayed in the tube cooling area of the screen. The system then becomes unresponsive to kV/mAs changes, prep/expose presses.…"

What does Class II mean?

FDA classifies recalls by relative degree of health hazard. Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.

Where was the product distributed?

FDA's distribution pattern field reads: "US Nationwide Distribution: TX, CA, OH, ID, WA, AZ"

Is the recall still ongoing?

FDA lists the status as Ongoing. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.

Where does this data come from?

openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.

Provenance

Source: openFDA device enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.