Barrx 360 Express Rfa Balloon Catheter (2018-02-08)

Recall Summary The Barrx 360 Express RFA Balloon Catheter is being recalled across Canada due to a medical device issue classified as Class I, the most serious type of recall. This device is used in medical procedures and was distributed throughout Canada. The specific technical reason for the recall relates to the device's safety or performance in medical applications.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2018-02-22

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/b5ec44a2-91f2-4db8-bded-203fbdf9edf0