Home/Recalls/CANADA-62623
Health CanadaType II

Pipeline Flex Embolization Device (2021-07-19)

Published: July 27, 2021Recall ID: 62623Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Pipeline Flex Embolization Device (2021-07-19)

Additional Source Details

FieldValue
N I D62623
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/pipeline-flex-embolization-device-2021-07-19
IssueMedical devices
Title Pipeline Flex Embolization Device (2021-07-19)
Archived0
CategoryMedical devices
Last updated2021-07-27
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert