Philips recalls Allura Xper FD20/15 X-ray systems due to internal component deterioration that could cause motorized movements to fail. Imaging remains functional but manual adjustments are still possible.
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.
Philips is recalling its Allura Xper FD20/15 X-ray systems because internal components like the CMOS battery and hard drive may deteriorate, causing motorized movements to stop working. This means the system might not function as intended during use, though imaging and manual adjustments remain available.
The system's internal components (CMOS battery, hard disk drive, and power supply) may deteriorate over time, causing motorized movements to become unavailable. Manual adjustments and imaging functions remain operational, so the risk is limited to specific movement mechanisms.
Medical facilities using Philips Allura Xper FD20/15 X-ray systems are most likely affected. Patients and staff using these systems during imaging procedures could be at risk if motorized movements fail.
Check for the product code 722058 on the system. The recall includes all units sold with this code, which have specific serial numbers listed in the official notice.
Look for the product code 722058 on the system to confirm if it is recalled.
The system may not perform as intended due to deterioration of internal components like the CMOS battery, hard disk drive, and power supply unit.
Manual movements of the stand and table remain available, so imaging functionality is still possible.
No, the system remains safe for use as imaging and manual adjustments are still functional.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2633-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-2633-2025 from Philips. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
