Home/Recalls/CANADA-61055
Health CanadaType II

Unify and Unify Assura, Fortify VR, DR, ST VR, ST DR, Assura VR, Assura DR Quadr...

Published: June 22, 2018Recall ID: 61055Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Unify and Unify Assura, Fortify VR, DR, ST VR, ST DR, Assura VR, Assura DR Quadra Assura, Assura MP, and Unify Quadra Cardiac Resynchronization Device, Tiered-therapy Cardioverter/Defibrillator (2018-06-01)

Additional Source Details

FieldValue
N I D61055
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/unify-and-unify-assura-fortify-vr-dr-st-vr-st-dr-assura-vr-assura-dr-quadra-assura
IssueMedical devices
Title Unify and Unify Assura, Fortify VR, DR, ST VR, ST DR, Assura VR, Assura DR Quadra Assura, Assura MP, and Unify Quadra Cardiac Resynchronization Device, Tiered-therapy Cardioverter/Defibrillator (2018-06-01)
Archived0
CategoryMedical devices
Last updated2018-06-22
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert