Home/Recalls/CANADA-53559
Health CanadaType II

IntraClude Intra-Aortic Occlusion Device (2015-05-08)

Published: June 15, 2015Recall ID: 53559Category: generalCountry: Canada

Reason for Recall / Hazard

Health products

Product Description & Identification

IntraClude Intra-Aortic Occlusion Device (2015-05-08)

Additional Source Details

FieldValue
N I D53559
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/intraclude-intra-aortic-occlusion-device-2015-05-08
IssueHealth products
Title IntraClude Intra-Aortic Occlusion Device (2015-05-08)
Archived1
CategoryMedical devices
Last updated2015-06-15
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert