Home/Recalls/CANADA-57510
Health CanadaType II

LiNA Librata-Endometrial Ablation Device (2017-10-06)

Published: October 20, 2017Recall ID: 57510Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

LiNA Librata-Endometrial Ablation Device (2017-10-06)

Additional Source Details

FieldValue
N I D57510
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/lina-librata-endometrial-ablation-device-2017-10-06
IssueMedical devices
Title LiNA Librata-Endometrial Ablation Device (2017-10-06)
Archived1
CategoryMedical devices
Last updated2017-10-20
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert