Philips recalls IntelliVue MX400 patient monitors with model 866060 due to potential failure to alarm when a Hamilton ventilator disconnects from the EC10 Module or IntelliBridge I/O board.
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 MX400 models with serial numbers starting with DE35174080 to DE7580B52H. The device may fail to alarm if a Hamilton ventilator is disconnected from the EC10 Module or IntelliBridge I/O board, which could lead to missed critical alerts during medical procedures.
The monitor may fail to alarm for 'No Device Data' when a Hamilton ventilator is disconnected from the EC10 Module or IntelliBridge I/O board. This could result in critical medical alerts being missed during patient monitoring, potentially leading to serious health risks.
Healthcare professionals using the IntelliVue MX400 patient monitor with model number 866060 are most at risk. This recall affects specific serial numbers listed in the official notice.
Check for the model number 866060 on the device. The serial numbers listed in the recall include DE35174080 to DE7580B52H. This product was sold by Philips North America.
Verify the model number on the device is 866060.
Reach out to Philips North America for specific instructions on how to address the issue.
The monitor may fail to alarm for 'No Device Data' when a Hamilton ventilator is disconnected from the EC10 Module or IntelliBridge I/O board.
Serial numbers starting with DE35174080 to DE7580B52H (as listed in the recall notice).
The recall record does not specify a remedy, so contact Philips North America for further instructions.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1107-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1107-2025 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.
