Class II
Medical Device Recall: MICRO-X Rover Mobile X-ray System, # MXU-RV35
Micro-X Ltd. · May 31, 2023
Reason for Recall
Shots were terminated by the mAs integrator; however, the 4 ms exposure time did not allow enough tolerance to achieve diagnostic exposures due to variations in hardware and how different timers are started.
Distribution
Worldwide and US Nationwide Distribution: NJ, PR, CA
States Affected
NATIONWIDE
Quantity Affected
5
Source: FDA (openFDA Device Enforcement)
Recall number: Z-0664-2025
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.