Its4850a Intellivue Telemetry System-main Uni

ITS4850A Intellivue Telemetry System-Main Unit Recall Summary Philips is recalling the ITS4850A Intellivue Telemetry System-Main Unit across Canada because the device may fail to display patient heart rhythm information, which could prevent healthcare providers from identifying serious cardiac conditions. This telemetry system is used in hospitals and clinical settings to monitor patients' heart activity. The recall affects all units of this model that were distributed in Canada.

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-03-31

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/645da6bf-70e5-43fe-afb0-42004e3433e8