Philips recalls Allura Xper FD20 OR Table models with specific product codes due to potential internal component failure. Motorized movements may become unavailable while manual adjustments and imaging functions remain operational.
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 FD20 OR Table medical imaging systems with certain product codes because internal components like the CMOS battery or hard drive may deteriorate. This could cause motorized movements to stop working, though manual adjustments and X-ray imaging functions still operate.
The system's internal components, including the CMOS battery and hard disk drive, can deteriorate over time. This deterioration may cause motorized movements to become unavailable, though manual adjustments and X-ray imaging functions remain functional.
Medical facilities using the Allura Xper FD20 OR Table with product codes 722023, 722035, or 722015 are most at risk. Patients and staff using these systems may experience temporary loss of motorized movement capabilities during procedures.
Check for product codes 722023, 722035, or 722015 on the device. These models were sold with specific 510(k) numbers and serial numbers listed in the recall notice.
Verify if motorized movements are functioning properly by attempting to move the table in both manual and motorized modes.
Philips recalls these models because internal components like the CMOS battery or hard disk drive may deteriorate, potentially causing motorized movements to stop working.
No. The recall does not require immediate discontinuation; manual movements and imaging functions remain operational.
Check the product code on your device to see if it matches the recalled models (722023, 722035, or 722015). If it does, monitor motorized movement functionality and contact Philips for further guidance.
We’ve drafted a message you can send Philips Medical Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-2628-2025 — Philips Medical Systems Philips Medical Systems Hello, I own a Philips Medical Systems that is covered by recall Z-2628-2025 from Philips Medical Systems. 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.
