Wallstent Endoprosthesis Tracheobronchial And Tracheobronchial Endoprosthesis With Unistep Plus Delivery System (2017-12-04)

Boston Scientific is recalling WALLSTENT Endoprosthesis devices used to treat blocked airways in the trachea and bronchi, along with their Unistep Plus delivery systems. The recall affects units distributed across Canada due to a defect in the medical device itself. This recall applies to healthcare facilities and patients who have received or may receive these stent devices.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-12-21

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/b10db38c-fb1a-4a7b-846a-7926e9131816