Home/Recalls/CANADA-52681
Health CanadaType III

SENSATION and SENSATION PLUS Intra-aortic Balloon Catheter (Demo) (2014-12-23)

Published: January 23, 2015Recall ID: 52681Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

SENSATION and SENSATION PLUS Intra-aortic Balloon Catheter (Demo) (2014-12-23)

Additional Source Details

FieldValue
N I D52681
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/sensation-and-sensation-plus-intra-aortic-balloon-catheter-demo-2014-12-23
IssueMedical devices
Title SENSATION and SENSATION PLUS Intra-aortic Balloon Catheter (Demo) (2014-12-23)
Archived1
CategoryMedical devices
Last updated2015-01-23
OrganizationMedical devices
Recall classType III

Overview

  • Recalling FirmMedical devices
  • Risk LevelType III
Official Agency Alert