Home/Recalls/CANADA-61647
Health CanadaType II

PIPELINE FLEX EMBOLIZATION DEVICE (2020-09-08)

Published: October 2, 2020Recall ID: 61647Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

PIPELINE FLEX EMBOLIZATION DEVICE (2020-09-08)

Additional Source Details

FieldValue
N I D61647
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/pipeline-flex-embolization-device-2020-09-08
IssueMedical devices
Title PIPELINE FLEX EMBOLIZATION DEVICE (2020-09-08)
Archived0
CategoryMedical devices
Last updated2020-10-02
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert