Home/Recalls/CANADA-73122
Health CanadaType II

Capiox FX25 Hollow Fiber Oxygenator With Integrated Arterial Filter

Published: March 9, 2023Recall ID: 73122Category: generalCountry: Canada

Reason for Recall / Hazard

Performance

Product Description & Identification

Capiox FX25 Hollow Fiber Oxygenator With Integrated Arterial Filter

Additional Source Details

FieldValue
N I D73122
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/capiox-fx25-hollow-fiber-oxygenator-integrated-arterial-filter
IssuePerformance
TitleCapiox FX25 Hollow Fiber Oxygenator With Integrated Arterial Filter
ProductCapiox FX25 Hollow Fiber Oxygenator With Integrated Arterial Filter
Archived0
CategoryCardiovascular
Last updated2023-03-09
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert