Iom Sensis Hemodynamic Application (2017-04-17)

Axiom Sensis Hemodynamic Application Recall The Axiom Sensis Hemodynamic Application, a medical device software used to monitor blood flow and pressure, has been recalled across Canada. The recall was issued due to safety concerns with the device itself. This recall affects all users of this application in Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2017-06-05
Status
Closed
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/70512b1a-51bd-49df-bb15-5c3e02ad3b32