Philips recalls Allura Xper FD20 OR Table models 722015, 722023, and 722035 due to potential battery depletion causing system shutdown without warning. Affected units may not start properly.
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.
Philips is recalling all Allura Xper FD20 OR Table models (722015, 722023, 722035) because the BIOS battery may deplete faster than expected, causing the system to stop starting without warning. This could lead to interrupted medical procedures if the device is used in a clinical setting.
The BIOS battery in these devices may deplete faster than designed, causing the system to halt during startup without any user warnings. This could interrupt medical procedures if the device is needed during critical operations.
Medical facilities using the Allura Xper FD20 OR Table with the specified model numbers are most at risk. Patients undergoing procedures with this equipment may be affected if the device fails to start.
Check for model numbers 722015, 722023, or 722035 on the device. The recall covers all units sold with these model numbers, regardless of serial number.
Identify the model number on your device to confirm if it is 722015, 722023, or 722035.
The BIOS battery may deplete faster than initially anticipated during design, causing the system to stop starting without warning.
The recall does not specify a remedy, so contact Philips directly for guidance on next steps.
The recall states the system may not start, but no injuries have been reported. The risk is limited to potential interruptions in medical procedures.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0008-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-0008-2026 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.
