Philips recalls Cardiac Workstation 7000 (product number 860441) due to intermittent inaccurate heart rate data. Affected units have specific serial numbers listed in the recall notice.
Device will intermittently provide inaccurate data related to native heart rate.
Philips is recalling its Cardiac Workstation 7000 devices with product number 860441 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 heart rate data that is not accurate. This could lead to incorrect medical decisions if the device is used for heart monitoring purposes.
Healthcare professionals using the Cardiac Workstation 7000 for heart monitoring are most at risk. Patients receiving care through this device may be affected if the readings are inaccurate.
Check for the product number 860441 on the device. Affected units have specific serial numbers listed in the recall notice, which include many US and international serial numbers.
Look for the serial number on the device or its packaging to determine if it is affected.
Philips recalls the Cardiac Workstation 7000 with product number 860441 due to intermittent inaccurate heart rate data.
Check the device's serial number against the list of affected serial numbers provided in the recall notice.
The recall does not specify a remedy, so affected users should contact Philips 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-2956-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-2956-2026 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
