Home/Recalls/CANADA-57730
Health CanadaType II

Kyphx Bone Filler Device (2017-12-08)

Published: January 8, 2018Recall ID: 57730Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Kyphx Bone Filler Device (2017-12-08)

Additional Source Details

FieldValue
N I D57730
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/kyphx-bone-filler-device-2017-12-08
IssueMedical devices
Title Kyphx Bone Filler Device (2017-12-08)
Archived0
CategoryMedical devices
Last updated2018-01-08
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert