Home/Recalls/CANADA-60938
Health CanadaType II

IntraClude Intra-aortic Occlusion Device (2018-04-02)

Published: May 18, 2018Recall ID: 60938Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

IntraClude Intra-aortic Occlusion Device (2018-04-02)

Additional Source Details

FieldValue
N I D60938
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/intraclude-intra-aortic-occlusion-device-2018-04-02
IssueMedical devices
Title IntraClude Intra-aortic Occlusion Device (2018-04-02)
Archived0
CategoryMedical devices
Last updated2018-05-18
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert