Its4850a Intellivue Telemetry System-monitor

Summary Philips is recalling the ITS4850A IntelliVue Telemetry System-Monitor across Canada due to a performance issue. The device is used in healthcare settings to monitor patient vital signs wirelessly. This is classified as a Class I recall, meaning there is a reasonable probability that use of the product will cause serious injury or death.

Product
ITS4850A IntelliVue Telemetry System-Monitor
Reason
Performance
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2023-06-14
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/a07765d9-a5c7-4931-9d37-07a9f5ff5c22