Philips recalls IntelliVue Patient Monitor MX750 (product #866471) 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 its IntelliVue Patient Monitor MX750 model because it may not alarm properly. This could mean critical patient conditions go undetected, which is dangerous in medical settings.
The monitor may not sound an alarm when a patient's condition becomes critical. This means healthcare staff might not know to take action until it's too late, potentially causing serious harm.
Healthcare providers using the IntelliVue MX750 monitor are most at risk. Patients in hospitals or clinics using this monitor could be affected if the device fails to alert.
Check for the product number 866471 on the monitor. The recall covers all units sold with this specific product number.
Test the monitor to ensure it alarms when needed, as the device may not function properly.
The recall states the monitor may not alarm properly, which could lead to undetected critical patient conditions. This is a safety concern but does not mean the monitor is immediately dangerous.
Check for product number 866471 on the monitor. All units with this specific product number are affected.
The recall does not specify a remedy, so you should check if the monitor alarms properly and contact Philips if you have concerns.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0868-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-0868-2026 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.