Philips recalls Allura Xper FD20/15 OR Table models with battery that may deplete faster than expected, causing system shutdown without warning. Affected units have model number 722059.
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 FD20/15 OR Table models with model number 722059 because the battery may deplete faster than expected, causing the system to shut down without warning. This could lead to interrupted medical procedures if the system fails during use.
The BIOS battery may deplete faster than designed, causing the system to stop starting without any warning messages. This could interrupt medical procedures if the system fails during critical use. The hazard does not involve immediate physical injury to users.
Medical facilities using the Allura Xper FD20/15 OR Table with model number 722059 are most at risk. Patients undergoing procedures with this equipment could be affected if the system shuts down unexpectedly.
Check for model number 722059 on the device. Affected units were sold with specific 510(k) clearances including K102005, K130638, K130842, K133292, K141979, K162859, and K161563.
Look for model number 722059 on the device to confirm if it is affected.
The BIOS battery may deplete faster than expected during the design phase, causing the system to shut down without warning.
The system will stop starting without any user messages, potentially interrupting medical procedures.
The recall record does not specify a remedy or fix for this issue.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0011-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-0011-2026 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.
