Philips recalls IntelliVue MX550 patient monitors with model 866066 due to potential failure to alarm when a 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 MX550 models with serial numbers starting with DE671E. The device may fail to alarm when a ventilator disconnects from the EC10 Module or IntelliBridge I/O board, which could lead to undetected patient issues.
The monitor may not alarm for 'No Device Data' when a ventilator is disconnected from the EC10 Module or IntelliBridge I/O board. This could result in undetected patient issues if the monitor fails to alert healthcare staff.
Healthcare professionals using Philips IntelliVue MX550 patient monitors with model number 866066 are most at risk. Patients connected to these monitors may experience undetected issues if the alarm fails.
Check for model number 866066 on the device. Serial numbers start with DE671E or DE351869 or DE758Y. The recall includes specific serial numbers listed in the official notice.
Identify the model number on the device, which should be 866066 for recalled units.
Reach out to Philips customer support for assistance with the recall process.
The model number for the recalled units is 866066.
Check for model number 866066 and serial numbers starting with DE671E, DE351869, or DE758Y as listed in the official recall notice.
Contact Philips customer support for assistance with the recall process.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1110-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1110-2025 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.
