Home/Recalls/CANADA-76236
Health CanadaType II

Ambu® Vivasight™ 2 DLT

Published: October 2, 2024Recall ID: 76236Category: generalCountry: Canada

Reason for Recall / Hazard

Performance

Product Description & Identification

Ambu® Vivasight™ 2 DLT

Additional Source Details

FieldValue
N I D76236
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/ambur-vivasighttm-2-dlt
IssuePerformance
TitleAmbu® Vivasight™ 2 DLT
ProductAmbu® Vivasight™ 2 DLT
Archived0
CategoryAnaesthesiology
Last updated2024-10-02
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert