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Micro-X Recalls

10 recalls on record · October 5, 2022 to April 29, 2026 · Medical Devices

Recalls by year

22
24
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26

Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.

April 29, 2026Medical DevicesFDA
Micro-X Ltd. recalls Rover Mobile X-ray System Model/Catalog Number: MXU-RV35 and MXU-RV71
Hazard: X-Ray generator may malfunction resulting in the X-Ray being inoperable.
April 30, 2025Medical DevicesFDA
Micro-X Ltd. recalls Brand Name: Rover Product Name: Mobile X-ray System Model/Catalog Number:MXU-RV35 Product Description: Rover Mobile X
Hazard: Potential for internal fastening mechanism within generator of mobile x-Ray to fail.
April 30, 2025Medical DevicesFDA
Micro-X Ltd. recalls Brand Name: Rover Product Name: Mobile X-ray System Model/Catalog Number: MXU-RV71, MXU-RV35 Product Description: Rov
Hazard: Potential for internal fastening mechanism within generator of mobile x-Ray to fail.
April 23, 2025Medical DevicesFDA
Micro-X Ltd. recalls Brand Name: Rover Product Name: Mobile X-ray System Model/Catalog Number: MXU-RV35 Product Description: Rover Mobile
Hazard: Potential for early life x-ray tube failure for mobile x-ray system due to excessive thermal load on the anode.
April 23, 2025Medical DevicesFDA
Micro-X Ltd. recalls Brand Name: Rover Product Name: Mobile X-ray System Model/Catalog Number: MXU-RV71 Product Description: Rover Mobile
Hazard: Potential for early life x-ray tube failure for mobile x-ray system due to excessive thermal load on the anode.
December 18, 2024Medical DevicesFDA
Micro-X Ltd. recalls MICRO-X Rover Mobile X-ray System, # MXU-RV19
Hazard: 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.
December 18, 2024Medical DevicesFDA
Micro-X Ltd. recalls MICRO-X Rover Mobile X-ray System, # MXU-RV35; MICRO-X Rover Mobile X-ray System, # MXU-RV71
Hazard: Mobile x-ray system can report and deliver a lower post-exposure mAs value than what set by the operator.
December 18, 2024Medical DevicesFDA
Micro-X Ltd. recalls MICRO-X Rover Mobile X-ray System, # MXU-RV35
Hazard: 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.
December 4, 2024Medical DevicesFDA
Micro-X Ltd. recalls MICRO-X Rover Mobile X-ray System, # MXU-RV35
Hazard: Mobile x-ray system receiving/storage(operation) requirements to be followed: Temp:14 to 131(50 to 86) degrees F, RH:10% to 86%(30% to 60%) allow condensation dry time, Atmospheric Pressure:50kPa to 106 kPa(70kPa to 106kPa), Altitude:-102ft to 12,000 ft, (Maximum Gradient:9 degrees Fahrenheit), which mitigate risk of capacitor malfunction, unpredictable behavior, overheating, unintended start-up.
October 5, 2022Medical DevicesFDA
Micro-X Ltd. recalls MICRO-X ROVER MOBILE X-RAY SYSTEM, MXU-RV19
Hazard: Software calibration error with product equip with a Dose Area Product (DAP) meter. This results in the product displaying the incorrect DAP meter values which may impede radiation exposure management decisions
Micro-X Recalls | RecallWatchUSA