Philips recalls Allura Xper FD10 medical imaging systems with model numbers 722003, 722010, and 722026 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 FD10 medical imaging systems with model numbers 722003, 722010, and 722026. The BIOS battery may deplete faster than expected, causing the system to stop starting without any user messages.
The BIOS battery may deplete faster than anticipated during design. When the battery is depleted, the system stops starting and shows no user messages before failure. This could lead to interrupted imaging sessions but does not cause injury.
Medical imaging system users who own one of the recalled model numbers (722003, 722010, or 722026) are affected. The risk is low as the issue only causes system shutdown without warning, not immediate injury.
Check if your Allura Xper FD10 has model numbers 722003, 722010, or 722026. The product is sold by Philips Medical Systems Netherlands B.V.
Identify if your system has model numbers 722003, 722010, or 722026.
The BIOS battery may deplete faster than anticipated during design, causing the system to stop starting without user messages.
The recall record does not specify a remedy, so no action is required beyond checking if your model number is listed.
The recall states the system stops starting without warning but does not mention injury risk, so the danger level is low.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0002-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-0002-2026 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.
