Philips recalls Allura Xper FD20 Biplane OR Table models with serial numbers starting 64 or 236 due to potential internal component deterioration. This may cause motorized movements to fail, but 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 its Allura Xper FD20 Biplane and OR Table models because internal components like the CMOS battery or hard drive could deteriorate over time. This might cause motorized movements to stop working, though manual adjustments and X-ray imaging functions still remain available.
The system's internal components, including the CMOS battery and hard disk drive, may deteriorate over time. If this happens, motorized movements of the table or stand could become unavailable, though manual adjustments and X-ray imaging functions would still work.
Medical facilities using the Allura Xper FD20 Biplane or OR Table models with specific serial numbers (starting with 64 or 236) are most at risk. Patients and staff using these systems could face temporary loss of motorized movement features during procedures.
Check the serial number on the product, which starts with '64' for model (1)722020 or '236' for model (2)722025. These models were sold with specific product codes and associated 510(k) numbers.
Look for the serial number starting with '64' or '236' on the product.
Philips recalls these models because internal components like the CMOS battery or hard disk drive may deteriorate over time, potentially causing motorized movements to stop working.
No, you do not need to stop using it immediately. Manual adjustments and X-ray imaging functions remain available, so the product can be used with caution.
Check the serial number to see if it starts with '64' or '236'. If so, contact Philips for further instructions.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2629-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-2629-2025 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.
