Home/Recalls/CANADA-47991
Health CanadaType II

Berman Angiographic Balloon Catheter (2019-11-20)

Published: December 13, 2019Recall ID: 47991Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Berman Angiographic Balloon Catheter (2019-11-20)

Additional Source Details

FieldValue
N I D47991
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/berman-angiographic-balloon-catheter-2019-11-20
IssueMedical devices
Title Berman Angiographic Balloon Catheter (2019-11-20)
Archived0
CategoryMedical devices
Last updated2019-12-13
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert