Home/Recalls/CANADA-60906
Health CanadaType I

T2 Ankle Arthrodesis Nail, IEFT, Non-Sterile, T2 Femur System - Femoral Nails, T...

Published: May 4, 2018Recall ID: 60906Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

T2 Ankle Arthrodesis Nail, IEFT, Non-Sterile, T2 Femur System - Femoral Nails, T2 Tibial Nail System - Nail Standard (Sterile) and T2 Recon Nail System - Titanium (2018-04-24)

Additional Source Details

FieldValue
N I D60906
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/t2-ankle-arthrodesis-nail-ieft-non-sterile-t2-femur-system-femoral-nails-t2-tibial
IssueMedical devices
Title T2 Ankle Arthrodesis Nail, IEFT, Non-Sterile, T2 Femur System - Femoral Nails, T2 Tibial Nail System - Nail Standard (Sterile) and T2 Recon Nail System - Titanium (2018-04-24)
Archived0
CategoryMedical devices
Last updated2018-05-04
OrganizationMedical devices
Recall classType I

Overview

  • Recalling FirmMedical devices
  • Risk LevelType I
Official Agency Alert