Rapidpoint® 500e Blood Gas System

RAPIDPoint® 500e Blood Gas System Recall The RAPIDPoint® 500e Blood Gas System is being recalled in Canada due to a performance issue. This device is used in healthcare settings to analyze blood gas samples. The recall affects all units of this system distributed across Canada.

Product
RAPIDPoint® 500e Blood Gas System
Reason
Performance
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2023-10-12
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/0b2f41fa-f2ee-40c5-9fd9-83fb6b8eed17