Philips recalls Cardiac Workstation 5000 (product number 860439) due to potential inaccurate native heart rate data. Affected units include specific serial numbers listed in the recall.
Device will intermittently provide inaccurate data related to native heart rate.
Philips is recalling its Cardiac Workstation 5000 devices because they may provide inaccurate heart rate readings. This could lead to incorrect medical decisions if the device is used for heart monitoring.
The device may intermittently provide inaccurate native heart rate data, which could lead to incorrect medical decisions if the device is used for heart monitoring. This is a potential issue for healthcare professionals relying on the device for critical patient assessments.
Healthcare professionals using the Cardiac Workstation 5000 for heart monitoring are most likely affected. Patients using this device for cardiac care may also be impacted.
Check for the product number 860439 and specific serial numbers listed in the recall notice. The device is sold under Philips North America LLC.
Look for the serial number on the device label or documentation to confirm if it's affected.
The recall states the device may provide inaccurate heart rate data, so it's recommended to check if your device is affected before use.
Check the serial number against the list provided in the recall notice. Affected units have specific serial numbers starting with US42510185, US42510184, and others listed in the record.
The recall does not specify a remedy, so contact Philips directly for further instructions.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2955-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-2955-2026 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.
