Micro-x Ltd
A14 6 MAB Eastern Promenade, Tonsley South Australia, AU
Registered product codes
2 product codes
Recent MDR events
0 on file
No MDR events on file for this firm name.
Recalls
10 on file
- Open, ClassifiedApr 22, 2026
X-Ray generator may malfunction resulting in the X-Ray being inoperable.
View FDA record ↗ - Open, ClassifiedApr 24, 2025
Potential for internal fastening mechanism within generator of mobile x-Ray to fail.
View FDA record ↗ - Open, ClassifiedApr 24, 2025
Potential for internal fastening mechanism within generator of mobile x-Ray to fail.
View FDA record ↗ - Open, ClassifiedApr 16, 2025
Potential for early life x-ray tube failure for mobile x-ray system due to excessive thermal load on the anode.
View FDA record ↗ - Open, ClassifiedApr 16, 2025
Potential for early life x-ray tube failure for mobile x-ray system due to excessive thermal load on the anode.
View FDA record ↗ - Open, ClassifiedDec 12, 2024
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.
View FDA record ↗ - Open, ClassifiedDec 12, 2024
Mobile x-ray system can report and deliver a lower post-exposure mAs value than what set by the operator.
View FDA record ↗ - Open, ClassifiedDec 12, 2024
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.
View FDA record ↗ - Open, ClassifiedNov 27, 2024
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.
View FDA record ↗ - Open, ClassifiedSep 23, 2022
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
View FDA record ↗
Compliance history
Matched by FEI 3012855798.
FDA inspections
2 on file
- Official Action Indicated (OAI)May 23, 2024
Compliance: Devices · Citations posted
- Official Action Indicated (OAI)May 23, 2024
Postmarket Assurance: Devices · Citations posted
Inspection citations
5 on file
Top cited requirements
Compare to industry ↗- 21 CFR 806.10(a)(1)May 23, 2024
Report of risk to health
- 21 CFR 820.30(i)May 23, 2024
Design changes - Lack of or Inadequate Procedures
- 21 CFR 820.75(a)May 23, 2024
Lack of or inadequate process validation
- 21 CFR 820.100(a)May 23, 2024
Lack of or inadequate procedures
- 21 CFR 820.198(a)May 23, 2024
Lack of or inadequate complaint procedures
Compliance actions
0 on file
No warning letters or injunctions on file for this FEI number.
Import refusals
0 on file
No import refusals on file for this FEI number.