Philips recalls IntelliVue Multi-Measurement Module X3 (product 867030) due to potential failure to alarm during critical events. Affected units may not alert healthcare providers to emergencies.
Potential issue where the IntelliVue monitors did not alarm.
Philips is recalling its IntelliVue Multi-Measurement Module X:3 monitors because they may not alarm during critical medical events. This could delay emergency responses and put patients at risk if a health issue occurs.
The monitors may not alarm when critical health events occur, such as a patient's condition worsening. This could delay emergency responses and lead to serious health consequences if the patient requires immediate attention.
Healthcare providers using the IntelliVue Multi-Measurement Module X3 monitors are most at risk. Patients relying on these monitors for critical health monitoring could be affected if the device fails to alert.
Check for product number 867030 on the device. The recall includes all units sold with this specific product number.
Verify if your monitor has product number 867030.
The monitors may not alarm during critical health events, which could delay emergency responses.
Check for product number 867030 on the device.
The recall does not specify a remedy, so contact Philips directly for guidance.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0860-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-0860-2026 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.
