Medical Device Recall: MICRO-X Rover Mobile X-ray System, # MXU-RV19
Micro-X Ltd. · October 23, 2024
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.
Distribution
US Nationwide Distribution: TX, CA, OH, ID, WA, AZ
States Affected
NATIONWIDE
Quantity Affected
23
Source: FDA (openFDA Device Enforcement)
Recall number: Z-0666-2025
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.