medical MODERATE Updated 2024-12-18

Micro-X Ltd. recalls MICRO-X Rover Mobile X-ray System, # MXU-RV19

See all recalls from Micro-X Ltd. →

Recalled Product

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

Share this recall: Facebook X / Twitter WhatsApp Email

Hazard / Issue

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.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: 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.

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

Looking for a safe alternative?

Search Amazon for MICRO-X Rover Mobile X-ray →
View official government recall