Home/Recalls/CANADA-51230
Health CanadaType II

Femoral Arterial Cannula - Fem-Flex II and Duraflo II Fem-Flex II (2014-04-09)

Published: May 5, 2014Recall ID: 51230Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Femoral Arterial Cannula - Fem-Flex II and Duraflo II Fem-Flex II (2014-04-09)

Additional Source Details

FieldValue
N I D51230
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/femoral-arterial-cannula-fem-flex-ii-and-duraflo-ii-fem-flex-ii-2014-04-09
IssueMedical devices
Title Femoral Arterial Cannula - Fem-Flex II and Duraflo II Fem-Flex II (2014-04-09)
Archived1
CategoryMedical devices
Last updated2014-05-05
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert