Iom Sensis System Electrophysiology And Hemodynamic Application (2017-04-17)

Axiom Sensis System Recall Summary The Axiom Sensis System, a medical device used for heart rhythm and blood pressure monitoring during cardiac procedures, has been recalled across Canada. The recall is classified as Class I, which is the most serious type. This recall affects the devices that were distributed throughout Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-05-16

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/be6ecb3c-3246-4947-98be-6b0ac8c1bf18