Micro-X Ltd.: Medical Device Recall in 2024 - (Recall #: Z-0666-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

MICRO-X Rover Mobile X-ray System, # MXU-RV19

Product Classification:

Class II

Date Initiated: October 23, 2024

Date Posted: December 18, 2024

Recall Number: Z-0666-2025

Event ID: 95593

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. The only way to proceed is to suspend the patient, Exit Nexus DR and relogin and continue the exam.

Status: Ongoing

Product Quantity: 23

Code Information:

UDI-DI: 09357123000013. Serial Numbers: 262, 274, 320, 329, 237, 269, 271, 290, 292, 307, 310, 311, 312, 321, 322, 323, 327, 330, 331, 332, 333, 234, 266.

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated