Philips recalls IntelliVue MX450 patient monitors (product #866062) due to potential failure to alarm, risking missed critical alerts. Affected units may need repair or replacement.
Potential issue where the IntelliVue monitors did not alarm.
Philips is recalling IntelliVue MX45:0 patient monitors that may not sound alarms, which could lead to missed critical health alerts. This is serious because patient monitors are vital for detecting emergencies.
The monitors may fail to sound alarms when a patient's condition worsens, potentially missing critical health changes. This could lead to delayed treatment or serious health issues if not addressed.
Healthcare professionals using the IntelliVue MX450 patient monitors are most at risk. Patients in hospitals or clinics using these monitors could be affected.
Check for product number 866062 on the monitor. The recall applies to all units sold with this product number.
Test if the monitor sounds alarms when a simulated emergency occurs.
The monitors may not sound alarms when a patient's condition worsens, potentially missing critical health changes.
Check for product number 866062 on the monitor. The recall applies to all units sold with this product number.
The recall does not specify a remedy, so contact Philips for guidance on next steps.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0863-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-0863-2026 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.
