Philips recalls Allura Xper FD10 OR Table models with specific product codes due to potential internal component deterioration that may cause motorized movements to fail. Imaging functions remain operational 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 Allura Xper FD10 OR Table medical imaging systems with specific product codes because internal components like the CMOS battery or hard drive may deteriorate. This could prevent motorized movements from working, though manual adjustments and imaging functions remain available.
The system's internal components, including the CMOS battery and hard disk drive, can deteriorate over time. If this happens, motorized movements (like table adjustments) may stop working, though manual movements and imaging functions remain functional.
Medical facilities using Philips Allura Xper FD10 OR Table systems with product codes 722022 or 722033 are most at risk. Patients and staff who rely on motorized movements for imaging procedures may need to adjust their workflow.
Check for product codes 722022 or 722033 on the device. The recall covers specific models sold with these codes, which are identified by their unique serial numbers and 510(k) numbers.
Verify if your system has product codes 722022 or 722033 by checking the device label or documentation.
Test if motorized movements (table adjustments) work as expected; if not, contact Philips for further guidance.
The recall is due to potential deterioration of internal components like the CMOS battery or hard disk drive, which could cause motorized movements to fail.
No, the system remains safe for manual movements and imaging functions. However, if motorized movements stop working, contact Philips for assistance.
Contact Philips directly to determine if your system requires repair or adjustment, as the recall does not include a specific remedy.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2625-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-2625-2025 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.
