Home/Recalls/CANADA-63710
Health CanadaType II

Cardiosave System - Hybrid & Rescue Intra-Aortic Balloon Pump

Published: December 13, 2021Recall ID: 63710Category: generalCountry: Canada

Reason for Recall / Hazard

Manufacturing defect

Product Description & Identification

Cardiosave System - Hybrid & Rescue Intra-Aortic Balloon Pump

Additional Source Details

FieldValue
N I D63710
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/cardiosave-system-hybrid-rescue-intra-aortic-balloon-pump
IssueManufacturing defect
TitleCardiosave System - Hybrid & Rescue Intra-Aortic Balloon Pump
ProductCardiosave System - Hybrid & Rescue Intra-Aortic Balloon Pump
Archived0
CategoryCardiovascular
Last updated2021-12-13
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert