Home/Recalls/CANADA-72661
Health CanadaType II

Lina Librata, Endometrial Ablation Device

Published: February 7, 2023Recall ID: 72661Category: generalCountry: Canada

Reason for Recall / Hazard

Labelling and packaging

Product Description & Identification

Lina Librata, Endometrial Ablation Device

Additional Source Details

FieldValue
N I D72661
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/lina-librata-endometrial-ablation-device
IssueLabelling and packaging
TitleLina Librata, Endometrial Ablation Device
ProductLina Librata, Endometrial Ablation Device
Archived0
CategoryObstetrics and gynaecology
Last updated2023-02-07
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert