Home/Recalls/CANADA-57210
Health CanadaType I

Datascope Corp. Intra Aortic Balloon Pump (2017-07-20)

Published: July 28, 2017Recall ID: 57210Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Datascope Corp. Intra Aortic Balloon Pump (2017-07-20)

Additional Source Details

FieldValue
N I D57210
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/datascope-corp-intra-aortic-balloon-pump-2017-07-20
IssueMedical devices
Title Datascope Corp. Intra Aortic Balloon Pump (2017-07-20)
Archived1
CategoryMedical devices
Last updated2017-07-28
OrganizationMedical devices
Recall classType I

Overview

  • Recalling FirmMedical devices
  • Risk LevelType I
Official Agency Alert