Home/Recalls/CANADA-51172
Health CanadaType III

Cardiovascular Procedure Kits (2013-07-26)

Published: May 5, 2014Recall ID: 51172Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Cardiovascular Procedure Kits (2013-07-26)

Additional Source Details

FieldValue
N I D51172
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/cardiovascular-procedure-kits-2013-07-26
IssueMedical devices
Title Cardiovascular Procedure Kits (2013-07-26)
Archived1
CategoryMedical devices
Last updated2014-05-05
OrganizationMedical devices
Recall classType III

Overview

  • Recalling FirmMedical devices
  • Risk LevelType III
Official Agency Alert