Express Ld Iliac/biliary Premounted Stent System

Recall Summary The Express LD Iliac/Biliary Premounted Stent System is being recalled across Canada due to a medical device issue. This stent system is used in medical procedures to open blocked blood vessels or bile ducts. The recall affects all units of this product distributed in Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-01-12

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/0881989c-7468-4e07-bef1-fbd4bb35cb19