Philips recalls IntelliVue Patient Monitor MX450 model 866062 due to potential failure to alarm when Hamilton ventilator disconnects from EC10 Module. Affected units may not alert to device disconnection risks.
Potential failure to alarm for "No Device Data" INOP. The device to alarm after a Hamilton ventilator is disconnected from the EC10 Module or IntelliBridge I/O board.
Philips is recalling IntelliVue Patient Monitor MX450 models with serial numbers starting with DE35169761 or similar. The device might not alarm if a Hamilton ventilator is disconnected from the EC10 Module or IntelliBridge I/O board, which could lead to undetected disconnections during critical medical monitoring.
The monitor may fail to sound an alarm when a Hamilton ventilator is disconnected from the EC10 Module or IntelliBridge I/O board. This means the device won't alert healthcare staff if the ventilator becomes disconnected, potentially leading to undetected patient monitoring issues.
Healthcare professionals using the IntelliVue Patient Monitor MX450 model 866062 are most at risk. Patients connected to this monitor could face undetected ventilator disconnections.
Check for model number 866062 on the device. Serial numbers start with DE35169761 or similar patterns listed in the recall notice. The device was sold by Philips North America.
Look for serial numbers starting with DE35169761 or similar patterns listed in the recall notice.
Reach out to Philips North America for specific model information and next steps.
The IntelliVue Patient Monitor MX450 model 866062 may fail to alarm when a Hamilton ventilator is disconnected from the EC10 Module or IntelliBridge I/O board, which could lead to undetected disconnections.
Check the device serial number against the list provided in the recall notice. Contact Philips North America for specific instructions.
The recall states a potential failure to alarm, but the official notice does not specify that this could cause serious injury or death in normal use.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1108-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1108-2025 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.
