Home/Recalls/CANADA-58561
Health CanadaType II

Cardiosave Hybrid IABP (2018-09-26)

Published: November 2, 2018Recall ID: 58561Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Cardiosave Hybrid IABP (2018-09-26)

Additional Source Details

FieldValue
N I D58561
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/cardiosave-hybrid-iabp-2018-09-26
IssueMedical devices
Title Cardiosave Hybrid IABP (2018-09-26)
Archived0
CategoryMedical devices
Last updated2018-11-02
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert