Philips recalls Allura Xper FD10 OR Table models with serial numbers starting with 1 or 6. The BIOS battery may deplete faster than expected, causing the system to stop starting 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 FD10 OR Table medical imaging devices with specific model numbers and serial numbers. The recall is due to a potential issue where the battery may deplete faster than expected, causing the system to stop starting without warning to the user.
The BIOS battery in these devices may deplete faster than expected during the design phase. When the battery runs out, the system stops starting without any user messages or warnings.
Medical facilities using Philips Allura Xper FD10 OR Table models with serial numbers starting with 1 or 6 are most at risk. This recall affects the specific model numbers and serial numbers listed in the notice.
Check for model number 722033 and serial numbers starting with 1 or 6 on the device. This recall applies to specific medical imaging equipment sold under the Philips brand.
Identify the model number (722033) and serial number (starting with 1 or 6) on your device.
The BIOS battery may deplete faster than expected, causing the system to stop starting without warning to the user.
Check the model number and serial number to confirm if your device is affected. The recall does not specify a remedy.
The recall record does not mention any 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-0004-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-0004-2026 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.
