Philips recalls Allura Xper FD10/10 models with serial numbers starting with 361-533. The BIOS battery may deplete faster than designed, 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 FD10/10 medical imaging systems with specific model numbers and serial ranges. The BIOS battery may deplete faster than expected, causing the system to stop starting without warning to users.
The BIOS battery may deplete faster than initially designed during the system's operation. When the battery is depleted, the system will stop starting without any user messages or warnings.
Medical imaging professionals who own or use the recalled Allura Xper FD10/10 systems with model numbers 722005, 722011, or 722027. The risk is low as the issue only affects system startup and not patient safety.
Check for model numbers 722005, 722011, or 722027 on the device. The serial numbers start with specific ranges listed in the recall notice.
Identify the model number on your Allura Xper FD10/10 device to confirm if it is in the recalled range.
The BIOS battery may deplete faster than initially designed, causing the system to stop starting without warning.
Check for model numbers 722005, 722011, or 722027 on your device. The serial numbers are listed in the recall notice.
The recall does not require immediate action, but you should check your device model to confirm if it is affected.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0003-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-0003-2026 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.
