Home/Recalls/CANADA-55742
Health CanadaType III

VANGUARD KNEE SYSTEM FEMORAL AUGMENT (2016-08-12)

Published: August 19, 2016Recall ID: 55742Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

VANGUARD KNEE SYSTEM FEMORAL AUGMENT (2016-08-12)

Additional Source Details

FieldValue
N I D55742
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/vanguard-knee-system-femoral-augment-2016-08-12
IssueMedical devices
Title VANGUARD KNEE SYSTEM FEMORAL AUGMENT (2016-08-12)
Archived1
CategoryMedical devices
Last updated2016-08-19
OrganizationMedical devices
Recall classType III

Overview

  • Recalling FirmMedical devices
  • Risk LevelType III
Official Agency Alert