Semislip Guidewire

Semislip Guidewire Recall Summary Semislip Guidewires are being recalled in Canada due to a quality or safety issue with the device. This recall affects all Semislip Guidewire products distributed across Canada. The devices are used in medical procedures and the issue has been classified as a Class I recall, which indicates a serious problem.

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2016-12-16

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/fa4ef202-532e-46d7-a7e8-d1eb3609918c