Allura Xper FD Allura Xper FD10 OR Table (REF 722022)Recalls & reported problems

Summary

The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 00884838059078), received between Dec 1, 2022 and Nov 20, 2025 — classified as 1 injury, 5 malfunctions.

The most frequently reported specific device problem is “Radiation Output Failure” (3 reports).

5 FDA recall records name this device's identifier, 5 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Recalls naming this device

1. Apr 30, 2026Class IIOpen, Classified

   It was identified that HDDs used in the PCs of Azurion and Allura systems may show a decrease in performance as they age, particularly beyond six years of service. Issues with an HDD may, depending on the specific system PC in which the affected HDD is installed, result in loss of imaging functionality. Additionally, in Allura systems, this may lead to loss of motorized movement, or loss of data. In some cases, a system restart may temporarily restore functionality.

   Z-2259-2026 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

2. Mar 3, 2026Class IIOpen, Classified

   Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.

   Z-1667-2026 · Root cause: Device Design · Recall details · FDA record ↗

3. Mar 3, 2026Class IIOpen, Classified

   Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.

   Z-1668-2026 · Root cause: Device Design · Recall details · FDA record ↗

4. Sep 3, 2025Class IIOpen, Classified

   Systems may not perform as intended due to the deterioration of certain internal components (the CMOS battery, hard disk drive, and/or power supply unit). If this deterioration occurs, motorized movements of the system will become unavailable. Manual movements of the stand (longitudinal, transversal and rotational for ceiling mounted systems and rotational for floor mounted systems) and table longitudinal movements remain available. Imaging (X-ray) functionality remains available.

   Z-2625-2025 · Root cause: Device Design · Recall details · FDA record ↗

5. Sep 3, 2025Class IIOpen, Classified

   The BIOS battery may deplete faster than initially anticipated during the design phase. When the battery is depleted, the start-up process of the system will be halted, and the system will not start. No user messages are shown before the battery is low on power or depleted.

   Z-0004-2026 · Root cause: Device Design · Recall details · FDA record ↗

Most reported problems

Recent adverse event reports

The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.

• MalfunctionNov 20, 2025Activation Failure; Activation Failure

  IT WAS REPORTED TO PHILIPS THAT THE SYSTEM FAILED TO BOOT AND THE IPPC MODULE WAS NOT FUNCTIONING ON AN ALLURA XPER FD10 OR TABLE. 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 23607280 ↗
• MalfunctionSep 9, 2025No Display/Image; No Display/Image

  IT WAS REPORTED TO PHILIPS THAT THE FLUOROSCOPY SCREEN WENT BLACK WHEN THE PEDAL WAS PRESSED ON A ALLURA XPER FD10 OR TABLE. 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 23005670 ↗
• InjuryMay 19, 2023Difficult or Delayed Positioning; Difficult or Delayed Positioning

  IT HAS BEEN REPORTED TO PHILIPS THAT THE ALLURA XPER FD10 OR TABLE WAS STIFF TO MOVE. DUE TO CONSTANT USE THIS WAS REPORTED TO HAVE CAUSED STRAIN TO THE USER'S WRIST AND ARM RESULTING IN HARM. THE DEVICE WAS INSIDE OF CLINICAL USE AT THE TIME OF THE EVENT. NO HARM TO THE PATIENT WAS REPORTED TO PHILIPS. TO DATE, NO FURTHER INFORMATION WAS RECEIVED. WE ARE CONSERVATIVELY REPORTING THIS EVENT AS THE INVESTIGATION IS ONGOING. A FOLLOW UP REPORT WILL BE SUBMITTED WHEN FURTHER INFORMATION IS RECEIVED.

  Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions

  MAUDE report 16961989 ↗
• MalfunctionMar 23, 2023Radiation Output Failure; Radiation Output Failure

  IT HAS BEEN REPORTED TO PHILIPS THAT FLUOROSCOPY STOPPED WORKING INTERMITTENTLY. THE ISSUE WAS FOUND DURING CLINICAL USE. NO HARM HAS BEEN REPORTED TO PHILIPS. PHILIPS HAS STARTED AN INVESTIGATION OF THIS COMPLAINT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16596006 ↗
• MalfunctionDec 20, 2022Radiation Output Failure; Radiation Output Failure

  IT HAS BEEN REPORTED TO PHILIPS THAT EXPOSURE WAS NOT POSSIBLE. IT IS UNKNOWN IF THE SYSTEM WAS IN CLINICAL USE. NO HARM HAS BEEN REPORTED TO PHILIPS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16014066 ↗
• MalfunctionDec 1, 2022Radiation Output Failure; Radiation Output Failure

  IT HAS BEEN REPORTED TO PHILIPS THAT THE FOOTSWITCH AND FLUOROSCOPY WAS NOT FUNCTIONING. THE ISSUE WAS FOUND DURING CLINICAL USE. NO HARM HAS BEEN REPORTED TO PHILIPS. PHILIPS HAS STARTED AN INVESTIGATION OF THIS COMPLAINT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15893516 ↗