Its4850a Intellivue Telemetry System (2020-02-28)

Recall Summary Philips is recalling the ITS4850A Intellivue Telemetry System due to a medical device issue. This patient monitoring system was distributed across Canada. The FDA classified this as a Class I recall, which indicates a serious potential health risk.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2020-03-13
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/045ac081-9753-482f-8a68-d66d6317d074