Home/Recalls/CANADA-44381
Health CanadaType III

Express LD Iliac/Biliary Premounted Stent System

Published: January 12, 2017Recall ID: 44381Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Express LD Iliac/Biliary Premounted Stent System

Additional Source Details

FieldValue
N I D44381
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/express-ld-iliacbiliary-premounted-stent-system
IssueMedical devices
Title Express LD Iliac/Biliary Premounted Stent System
Archived1
CategoryMedical devices
Last updated2017-01-12
OrganizationMedical devices
Recall classType III

Overview

  • Recalling FirmMedical devices
  • Risk LevelType III
Official Agency Alert