Philips recalls Allura Xper FD20 Biplane models 722008 and 722013 due to potential 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 Biplane medical imaging devices with model numbers 722008 and 722013. 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 may deplete faster than designed, causing the system to stop working without any warning messages. This could lead to interrupted medical imaging procedures if the device is used during critical operations.
Medical professionals using the Allura Xper FD20 Biplane imaging system with model numbers 722008 or 722013 are most at risk if the device fails during critical procedures.
Check for model numbers 722008 or 722013 on the device. The product was sold with associated 510(k) clearances K102005, K130638, K130842, and others.
Look for model numbers 722008 or 722013 on the device.
The BIOS battery may deplete faster than initially anticipated, causing the system to shut down without warning messages.
The recall record does not specify a remedy, so no action is required beyond checking if your device has the model numbers 722008 or 722013.
The recall indicates a potential for system shutdown without warning, which could disrupt medical procedures. However, no specific injuries are mentioned in the recall record.
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-0006-2026 — Philips Medical Systems Philips Medical Systems Hello, I own a Philips Medical Systems that is covered by recall Z-0006-2026 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.
