Intellivue Mx Patient Monitor System-intellibridge Module Ec10

Philips Breast Coils Recall Philips Breast Coils used in MRI imaging equipment are being recalled across Canada due to performance issues. This is a Class I recall, indicating a serious problem that could affect diagnostic accuracy. The recall applies to all Philips Breast Coils distributed in Canada.

Product

IntelliVue MX Patient Monitor System-IntelliBridge Module EC10

Reason

Device performance issue

Classification

Class II

Category

medical device recall

Country

Canada

Agency

HC-DEVICES

Recall date

2026-03-11

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/90a9024d-5923-4fc0-a0bb-d39889bc77ff