Philips recalls IntelliVue Patient Monitor MX700 (product #865241) due to potential failure to alarm. Affected units may not alert to critical patient conditions.
Potential issue where the IntelliVue monitors did not alarm.
Philips is recalling IntelliVue Patient Monitor MX700 models that may not alarm properly. This could mean critical patient conditions go undetected, putting users at risk.
The monitor may fail to sound alarms when critical patient conditions occur. This could lead to undetected medical emergencies if the monitor doesn't alert healthcare staff.
Healthcare professionals using the IntelliVue MX700 patient monitor are most at risk. Patients in hospitals or clinics using this monitor could be affected.
Check for product number 865241 on the monitor. All units with this product number are affected. The monitor has a unique identifier starting with 00884838029088.
Test the monitor's alarm system to ensure it sounds when critical conditions occur.
The recall indicates potential failure to alarm, so it may not be safe to use without testing.
Check for product number 865241 on the monitor. All units with this number are affected.
Test the monitor's alarm system to ensure it functions properly. If it fails, 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-0867-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-0867-2026 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.
