Philips recalls Allura Xper FD20/15 medical imaging devices with model 722058 due to potential BIOS battery depletion causing system shutdown without warning.
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 Allura Xper FD20/15 medical imaging devices with model number 722058 because the BIOS battery may deplete faster than expected, causing the system to shut down without warning. This could disrupt medical procedures if the device is used during critical operations.
The BIOS battery in these devices may deplete faster than designed, causing the system to stop working without any warning messages. This could lead to interruptions in medical procedures if the device is needed during critical operations.
Medical facilities using Philips Allura Xper FD20/15 devices with model number 722058 are affected. Patients undergoing procedures with this device may be at risk if the system unexpectedly shuts down during critical moments.
Check for model number 722058 on the device. The recall covers specific serial numbers listed in the official notice. This device is used in medical imaging settings.
Look for the model number 722058 on the device label to confirm if it is affected.
The BIOS battery may deplete faster than expected, causing the system to shut down without warning messages.
Check the model number on the device. If it is 722058, contact Philips for further instructions.
The recall indicates a potential risk of system shutdown without warning, but it is not expected to cause serious injury under normal use conditions.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0010-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-0010-2026 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.
