Home/Recalls/CANADA-50930
Health CanadaType II

Patient Data Module (2013-11-11)

Published: January 6, 2014Recall ID: 50930Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Patient Data Module (2013-11-11)

Additional Source Details

FieldValue
N I D50930
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/patient-data-module-2013-11-11-0
IssueMedical devices
Title Patient Data Module (2013-11-11)
Archived1
CategoryMedical devices
Last updated2014-01-06
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert