Zur Cx Peripheral Coil System (2019-11-26)

Azur CX Peripheral Coil System Recall The Azur CX Peripheral Coil System is being recalled across Canada due to a medical device issue. This device is used for vascular procedures. The recall is classified as Class I, which is the most serious type of recall.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2019-12-13
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/3e2311be-c9dd-4203-b9b6-0c9568d405c8