Philips recalls Cardio Vascular-Allura Centron model 722400 due to potential battery depletion causing system shutdown without warning. Affected units may not start properly.
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 its Cardio Vascular-Allura Centron medical device model 722400 because the BIOS battery may deplete faster than expected, causing the system to shut down without warning. This could prevent the device from starting properly, which is critical for medical use.
The BIOS battery in the device may deplete faster than designed, causing the system to stop starting without any user warnings. This could lead to the device failing to operate when needed, potentially disrupting medical monitoring or diagnostics.
Healthcare facilities using the Cardio Vascular-Allura Centron model 722400 are most at risk. This device is used in medical settings for cardiovascular monitoring and diagnostics.
Check for the model number 722400 on the device. The recall affects units sold with specific 510(k) clearances listed in the record. Serial numbers are provided in the detailed list.
Verify if the system starts properly when powered on. If it fails to start, the device is affected.
The BIOS battery may deplete faster than expected, causing the system to shut down without warning and fail to start properly.
Check for the model number 722400. Affected units have specific serial numbers listed in the recall notice.
The recall does not specify a remedy, so contact Philips Medical Systems directly for guidance.
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-0015-2026 — Philips Medical Systems Philips Medical Systems Hello, I own a Philips Medical Systems that is covered by recall Z-0015-2026 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.
