Home/Recalls/CANADA-64290
Health CanadaType II

Ambu Vivasight 2 Dlt Kit

Published: June 20, 2022Recall ID: 64290Category: generalCountry: Canada

Reason for Recall / Hazard

Performance

Product Description & Identification

Ambu Vivasight 2 Dlt Kit

Additional Source Details

FieldValue
N I D64290
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/ambu-vivasight-2-dlt-kit
IssuePerformance
TitleAmbu Vivasight 2 Dlt Kit
ProductAmbu Vivasight 2 Dlt Kit
Archived0
CategoryAnaesthesiology
Last updated2022-06-20
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert