Philips recalls IntelliBridge EC10 Module (model 865115) due to potential failure to alarm when a Hamilton ventilator disconnects. This could lead to undetected disconnections. Affected units have specific serial numbers listed in the recall.
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 its IntelliBridge EC10 Module (model 865115) because it may fail to alarm when a Hamilton ventilator is disconnected from the module. This could result in undetected disconnections, which is a safety risk for medical equipment users. If you own this model, you should check your serial number against the list provided in the recall.
The module may fail to alarm when a Hamilton ventilator is disconnected from it. This means that if the ventilator is unplugged, the system won't alert the user, potentially leading to undetected disconnections and safety risks during medical procedures.
Medical equipment users who have the IntelliBridge EC10 Module (model 865115) with the listed serial numbers are most at risk. This recall affects hospital and clinical settings where the module is used with Hamilton ventilators.
Check if your IntelliBridge EC10 Module has the model number 865115 and one of the serial numbers listed in the recall (e.g., DE57029003, DE57028993, etc.). The recall includes specific serial numbers provided in the official notice.
Compare your module's serial number with the list of affected serial numbers provided in the recall notice.
The model number is 865115.
Check your serial number against the list of affected serial numbers provided in the recall notice.
The recall does not specify a remedy, so you should contact Philips directly 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-1106-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1106-2025 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.
