Home/Recalls/CANADA-62002
Health CanadaType II

EPIQ ULTRASOUND SYSTEM (2020-12-24)

Published: January 15, 2021Recall ID: 62002Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

EPIQ ULTRASOUND SYSTEM (2020-12-24)

Additional Source Details

FieldValue
N I D62002
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/epiq-ultrasound-system-2020-12-24
IssueMedical devices
Title EPIQ ULTRASOUND SYSTEM (2020-12-24)
Archived0
CategoryMedical devices
Last updated2021-01-15
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert