Home/Recalls/CANADA-55178
Health CanadaType I

RE-STERILZED ANGIODYNAMICS SOFT-VU OMNI FLUSH ANGIOGRAPHIC CATHETER (2016-06-01)

Published: July 12, 2016Recall ID: 55178Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

RE-STERILZED ANGIODYNAMICS SOFT-VU OMNI FLUSH ANGIOGRAPHIC CATHETER (2016-06-01)

Additional Source Details

FieldValue
N I D55178
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/sterilzed-angiodynamics-soft-vu-omni-flush-angiographic-catheter-2016-06-01
IssueMedical devices
Title RE-STERILZED ANGIODYNAMICS SOFT-VU OMNI FLUSH ANGIOGRAPHIC CATHETER (2016-06-01)
Archived1
CategoryMedical devices
Last updated2016-07-12
OrganizationMedical devices
Recall classType I

Overview

  • Recalling FirmMedical devices
  • Risk LevelType I
Official Agency Alert