Home/Recalls/CANADA-50543
Health CanadaType II

Vivid E9 Ultrasound System (2013-10-02)

Published: October 25, 2013Recall ID: 50543Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Vivid E9 Ultrasound System (2013-10-02)

Additional Source Details

FieldValue
N I D50543
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/vivid-e9-ultrasound-system-2013-10-02
IssueMedical devices
Title Vivid E9 Ultrasound System (2013-10-02)
Archived1
CategoryMedical devices
Last updated2013-10-25
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert