Philips recalls IntelliVue MX600 patient monitors that may not alarm properly. Affected units have product number 865242. Contact Philips for details.
Potential issue where the IntelliVue monitors did not alarm.
Philips is recalling IntelliVue MX600 patient monitors that may not alarm properly. This could lead to missed critical patient alerts, which is dangerous in medical settings.
The monitors may fail to alarm when a patient's condition becomes critical. This means critical health changes might not be detected, potentially delaying life-saving interventions.
Healthcare providers using the IntelliVue MX600 patient monitors are most at risk. Patients in hospitals or clinics using these monitors could be affected.
Check for product number 865242 on the monitor. The recall covers all units with this specific product number and serial numbers.
Verify if your IntelliVue MX600 monitor has product number 865242.
The monitors may not alarm properly, which could lead to missed critical patient alerts.
Check if your monitor has product number 865242. Contact Philips for further instructions.
The recall record does not specify a remedy or fix.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0866-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-0866-2026 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.
