Interventional Workspot Interventional Workspot - 1Recalls & reported problems

Summary

The FDA's MAUDE database contains 24 adverse event reports that list this exact device (DI 00884838059191), received between Jan 11, 2021 and Nov 18, 2025 — classified as 24 malfunctions.

The most frequently reported specific device problem is “Activation Failure” (11 reports).

13 FDA recall records name this device's identifier, 12 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Recalls naming this device

1. Jan 13, 2025Open, Classified

   Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel

   Z-1080-2025 · Root cause: Device Design · FDA record ↗

2. Jan 13, 2025Open, Classified

   Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel

   Z-1077-2025 · Root cause: Device Design · FDA record ↗

3. Jan 13, 2025Open, Classified

   Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel

   Z-1081-2025 · Root cause: Device Design · FDA record ↗

4. Jan 13, 2025Open, Classified

   Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel

   Z-1078-2025 · Root cause: Device Design · FDA record ↗

5. Aug 22, 2024Open, Classified

   Potential Detachment of the Cable Hose Carrier (due to broken plastic and/or bolts) which May Result in Parts Falling and/or Part of the Cable Hose Dropping, and result in injury.

   Z-3166-2024 · Root cause: Device Design · FDA record ↗

6. Jan 2, 2024Open, Classified

   Framegrabber card may not perform as intended. Monitor may show no viewports, or show one or more viewports may show no image, a distorted image, or a frozen image. Switching between viewports on the monitor may not be possible. Issue may result in delay of procedure.

   Z-1145-2024 · Root cause: Process design · FDA record ↗

7. Jan 2, 2024Open, Classified

   Framegrabber card may not perform as intended. Monitor may show no viewports, or show one or more viewports may show no image, a distorted image, or a frozen image. Switching between viewports on the monitor may not be possible. Issue may result in delay of procedure.

   Z-1144-2024 · Root cause: Process design · FDA record ↗

8. Jan 2, 2024Open, Classified

   Disk Bay may not perform as intended. System may stop functioning and imaging may not be possible, resulting in delay of procedure.

   Z-1151-2024 · Root cause: Process design · FDA record ↗

9. Jan 2, 2024Open, Classified

   Dual In-Line Memory Modules (DIMMs) may not perform as intended. System may stop functioning and imaging may not be possible, resulting in delay of procedure.

   Z-1156-2024 · Root cause: Process design · FDA record ↗

10. Jan 2, 2024Open, Classified

    Disk Bay may not perform as intended. System may stop functioning and imaging may not be possible, resulting in delay of procedure.

    Z-1152-2024 · Root cause: Process design · FDA record ↗

11. Dec 12, 2023Open, Classified

    System may exhibit a loss of imaging functionality and data due to an issue which can cause the system to continuously restart. If the issue occurs during a procedure, there may be a delay and/or abortion of the procedure.

    Z-0835-2024 · Root cause: Under Investigation by firm · FDA record ↗

12. Jun 12, 2023Open, Classified

    The bolts supporting the FlexMove Carriage may become loose and/or break, and cracks may appear in the suspension rail of the FlexMove Carriage.

    Z-2283-2023 · Root cause: Component design/selection · FDA record ↗

13. Nov 19, 2021Terminated

    Set screws securing the two gliding rods of the Extra Monitors (called 7th and 8th monitor) mounted on the Monitor Ceiling Suspension (MCS) can come loose, the Extra monitors might disengage from the Mounting Ceiling Suspension structure and fall down, may lead to patient, user or service engineer harm that may require medical intervention.

    Z-0416-2022 · Root cause: Other · FDA record ↗

Most reported problems

Recent adverse event reports

The 24 most recent of 24 reports, in the reporter's own words as published by the FDA.

• MalfunctionNov 18, 2025Activation Failure; Activation Failure

  IT WAS REPORTED TO PHILIPS THAT FLEXVISION PC FAILED TO START; SOFTWARE REINSTALLED ON A ALLURA XPER FD20/20. THE CLINICAL USE OF THE SYSTEM WAS OUTSIDE OF USE. THERE WAS NO REPORTED PATIENT OR USER HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23589848 ↗
• MalfunctionNov 13, 2025Activation Failure; Activation Failure

  IT WAS REPORTED TO PHILIPS THAT THE SYSTEM'S FLEXVISION COMPUTER WAS UNABLE TO BOOT, STALLING AT 00:00. THE DEVICE WAS OUTSIDE OF CLINICAL USE AT THE TIME OF REPORTED EVENT. NO HARM WAS REPORTED TO PHILIPS. PHILIPS HAS STARTED AN INVESTIGATION OF THIS COMPLAINT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23548038 ↗
• MalfunctionOct 27, 2025Activation Failure; Activation Failure

  IT WAS REPORTED TO PHILIPS THAT UPS FAILURE CAUSED SYSTEM POWER ISSUES ON A ALLURA XPER FD10. THE CLINICAL USE OF THE SYSTEM WAS UNKNOWN. THERE WAS NO REPORTED PATIENT OR USER HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23393894 ↗
• MalfunctionSep 15, 2025Radiation Output Failure; Radiation Output Failure

  IT WAS REPORTED TO PHILIPS THAT A HIGH VOLTAGE CABLE FAILURE CAUSED IMAGING ERRORS ON AN ALLURA XPER FD20. THE CLINICAL USE OF THE SYSTEM WAS IN USE. THERE WAS NO REPORTED PATIENT OR USER HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23049248 ↗
• MalfunctionSep 9, 2025Activation Failure; Activation Failure

  IT WAS REPORTED TO PHILIPS THAT FLEX VISION TURNED OFF DURING A CASE, CAUSING IMAGE LOSS ON A ALLURA XPER FD20/15. THE CLINICAL USE OF THE SYSTEM WAS IN USE. THERE WAS NO REPORTED PATIENT OR USER HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23002065 ↗
• MalfunctionSep 2, 2025Radiation Output Failure; Radiation Output Failure

  IT WAS REPORTED TO PHILIPS THAT THE FOOT PEDALS INTERMITTENTLY FAIL, CAUSING LOSS OF FLUORO IMAGE ON A ALLURA XPER FD20. THE CLINICAL USE OF THE SYSTEM WAS IN USE. THERE WAS NO REPORTED PATIENT OR USER HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22932139 ↗
• MalfunctionAug 29, 2025Radiation Output Failure; Radiation Output Failure

  IT WAS REPORTED TO PHILIPS THAT IPPC FAILURE CAUSED AN INABILITY TO PERFORM X-RAYS ON AN ALLURA XPER FD20. THE CLINICAL USE OF THE SYSTEM WAS IN USE. THERE WAS NO REPORTED PATIENT OR USER HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22921170 ↗
• MalfunctionAug 27, 2025Activation Failure; Activation Failure

  IT WAS REPORTED TO PHILIPS THAT THE HOST PC FAILED TO BOOT, CAUSING SYSTEM STARTUP ISSUES ON AN ALLURA XPER FD10. THE CLINICAL USE OF THE SYSTEM WAS OUTSIDE OF USE. THERE WAS NO REPORTED PATIENT OR USER HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22902192 ↗
• MalfunctionAug 19, 2025Positioning Failure; Positioning Failure

  IT WAS REPORTED TO PHILIPS THAT THE SYSTEM'S GEOMETRY MOVEMENTS STOPPED. THE DEVICE WAS IN CLINICAL USE AT THE TIME OF THE EVENT. NO HARM WAS REPORTED TO PHILIPS. PHILIPS HAS STARTED AN INVESTIGATION OF THIS COMPLAINT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22840932 ↗
• MalfunctionJul 23, 2025Radiation Output Failure; Radiation Output Failure

  IT WAS REPORTED TO PHILIPS THAT IT DOES NOT START. THE IS CONNECTED TO A STARTUP ISSUE RELATED TO A ALLURA XPER FD20/20. THERE WAS NO REPORTED PATIENT OR USER HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22574536 ↗
• MalfunctionJul 10, 2025Activation Failure; Activation Failure

  IT WAS REPORTED TO PHILIPS THAT THE SYSTEM WAS UNABLE TO BOOT UP AFTER A POWER OUTAGE. THE DEVICE WAS OUTSIDE OF CLINICAL USE AT THE TIME OF REPORTED EVENT. NO HARM WAS REPORTED TO PHILIPS. PHILIPS HAS STARTED AN INVESTIGATION OF THIS COMPLAINT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22475914 ↗
• MalfunctionJul 8, 2025Activation Failure; Activation Failure

  IT WAS REPORTED TO PHILIPS THAT THE SYSTEM WAS UNABLE TO FULLY BOOT. THE DEVICE WAS NOT IN CLINICAL USE AT THE TIME OF THE EVENT. NO HARM TO THE PATIENT OR USER WAS REPORTED. PHILIPS HAS STARTED AN INVESTIGATION OF THIS COMPLAINT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22446789 ↗
• MalfunctionJun 30, 2025Activation Failure; Activation Failure

  IT WAS REPORTED TO PHILIPS THAT THE SYSTEM WOULD NOT BOOTUP. THE DEVICE WAS OUTSIDE OF CLINICAL USE AT THE TIME OF THE REPORTED EVENT. NO HARM WAS REPORTED TO PHILIPS. PHILIPS HAS STARTED AN INVESTIGATION OF THIS COMPLAINT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22358748 ↗
• MalfunctionJun 27, 2025Activation Failure; Activation Failure

  IT WAS REPORTED TO PHILIPS THAT THE SUITE COMPUTER AND FLEXVISION COMPUTER WAS UNABLE TO BOOT UP. THE DEVICE WAS OUTSIDE OF CLINICAL USE AT THE TIME OF THE EVENT. NO HARM TO THE PATIENT OR USER WAS REPORTED. PHILIPS HAS STARTED AN INVESTIGATION OF THIS COMPLAINT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22345507 ↗
• MalfunctionJun 17, 2025Radiation Output Failure; Radiation Output Failure

  IT WAS REPORTED TO PHILIPS THAT THE SYSTEM GAVE AN ALERT INDICATING FREE DISK SPACE WAS TOO LOW, PREVENTING EXPOSURE. THE DEVICE WAS IN CLINICAL USE AT THE TIME OF THE EVENT. NO HARM TO THE PATIENT OR USER WAS REPORTED. PHILIPS HAS STARTED AN INVESTIGATION OF THIS COMPLAINT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22245050 ↗
• MalfunctionMay 28, 2025Radiation Output Failure; Radiation Output Failure

  IT WAS REPORTED TO PHILIPS THAT DURING A PROCEDURE THE WIRED FOOTSWITCH STOPPED WORKING, UNABLE TO PERFORM EXPOSURE. THE DEVICE WAS INSIDE CLINICAL USE AT THE TIME OF REPORTED EVENT. NO HARM WAS REPORTED TO PHILIPS. PHILIPS HAS STARTED AN INVESTIGATION OF THIS COMPLAINT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22094168 ↗
• MalfunctionApr 24, 2025Positioning Failure; Positioning Failure

  IT WAS REPORTED TO PHILIPS THAT THE SYSTEM GAVE A REMOTE ALERT, WHICH CAN IMPACT SYSTEM GEOMETRY MOVEMENTS. NO HARM WAS REPORTED TO PHILIPS. PHILIPS HAS STARTED AN INVESTIGATION OF THIS COMPLAINT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21897322 ↗
• MalfunctionApr 3, 2025Positioning Failure; Positioning Failure

  IT WAS REPORTED TO PHILIPS THAT THE SYSTEM'S C-ARM WAS UNABLE TO MOVE. THE DEVICE WAS IN CLINICAL USE AT THE TIME OF THE EVENT. NO HARM TO THE PATIENT OR USER WAS REPORTED. PHILIPS HAS STARTED AN INVESTIGATION OF THIS COMPLAINT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21759754 ↗
• MalfunctionMar 21, 2025Detachment of Device or Device Component; Detachment of Device or Device Component

  IT WAS REPORTED TO PHILIPS THAT THE CEILING PROTECTIVE COVER FELL OFF. NO HARM WAS REPORTED TO PHILIPS. PHILIPS HAS STARTED AN INVESTIGATION OF THIS COMPLAINT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21661356 ↗
• MalfunctionDec 27, 2024Positioning Failure; Positioning Failure

  IT WAS REPORTED TO PHILIPS THAT THERE WAS A GEOMETRY MOVEMENT PROBLEM OF THE X-RAY TUBE. THE DEVICE WAS IN CLINICAL USE AT THE TIME OF THE REPORTED EVENT. NO HARM WAS REPORTED TO PHILIPS. PHILIPS HAS STARTED AN INVESTIGATION OF THIS COMPLAINT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21025967 ↗
• MalfunctionDec 3, 2024Activation Failure; Activation Failure

  IT WAS REPORTED TO PHILIPS THAT THE SYSTEM WOULD NOT BOOT UP. THE DEVICE WAS NOT IN CLINICAL USE AT THE TIME OF THE REPORTED EVENT. NO HARM TO THE PATIENT OR USER WAS REPORTED. PHILIPS HAS STARTED AN INVESTIGATION OF THIS COMPLAINT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20834127 ↗
• MalfunctionDec 2, 2024Activation Failure; Activation Failure

  IT WAS REPORTED TO PHILIPS THAT THE SYSTEM WAS UNABLE TO BOOT UP CORRECTLY. THE DEVICE WAS OUTSIDE OF CLINICAL USE AT THE TIME OF THE REPORTED EVENT. NO HARM WAS REPORTED TO PHILIPS. PHILIPS HAS STARTED AN INVESTIGATION OF THIS COMPLAINT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20816752 ↗
• MalfunctionNov 19, 2021Radiation Output Failure; Radiation Output Failure

  IT HAS BEEN REPORTED TO PHILIPS THAT DURING A PLANNED TREATMENT PROCEDURE THE WIRELESS FOOTSWITCH DID NOT WORK PROPERLY AND THE WIFI INDICATOR WAS RED. THE PROCEDURE WAS COMPLETED USING THE WIRED FOOTSWITCH. NO HARM TO THE PATIENT HAS BEEN REPORTED TO PHILIPS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12842746 ↗
• MalfunctionJan 11, 2021Application Program Freezes or Fails to Launch; Application Program Freezes or Fails to Launch

  IT HAS BEEN REPORTED TO PHILIPS THAT DURING AN EMERGENCY PROCEDURE FOR A STROKE PATIENT, THE CUSTOMER WAS NOT ABLE TO USE THE XPERCT FUNCTIONALITY OF THE SYSTEM. THE PROCEDURE WAS COMPLETED USING REGULAR CT. NO HARM TO THE PATIENT OR USER HAS BEEN REPORTED TO PHILIPS. PHILIPS HAS STARTED AN INVESTIGATION FOR THIS COMPLAINT.

  Patient problems: No Clinical Signs, Symptoms or Conditions; No Consequences Or Impact To Patient

  MAUDE report 11147367 ↗