Home/Recalls/CANADA-60852
Health CanadaType II

Vivid 7 Dimension Ultrasound System, Vivid E9 Ultrasound System, Vivid E95 and V...

Published: April 24, 2018Recall ID: 60852Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Vivid 7 Dimension Ultrasound System, Vivid E9 Ultrasound System, Vivid E95 and Vivid E90 (2018-03-28)

Additional Source Details

FieldValue
N I D60852
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/vivid-7-dimension-ultrasound-system-vivid-e9-ultrasound-system-vivid-e95-and-vivid-e90
IssueMedical devices
Title Vivid 7 Dimension Ultrasound System, Vivid E9 Ultrasound System, Vivid E95 and Vivid E90 (2018-03-28)
Archived0
CategoryMedical devices
Last updated2018-04-24
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert