Sensor Guidewire (2020-03-09)

Sensor Guidewire Recall Summary A medical device called a Sensor Guidewire has been recalled across Canada due to safety concerns. The recall is classified as Class I, meaning there is a serious risk of adverse health consequences. The device was distributed nationwide in Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2020-04-17

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/67f40efc-483a-4c1d-bd85-c9351680d15a