Home/Recalls/CANADA-63929
Health CanadaType I

Liquiband Fix8 Open Hernia Mesh Fixation Device

Published: February 14, 2022Recall ID: 63929Category: generalCountry: Canada

Reason for Recall / Hazard

Manufacturing defect

Product Description & Identification

Liquiband Fix8 Open Hernia Mesh Fixation Device

Additional Source Details

FieldValue
N I D63929
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/liquiband-fix8-open-hernia-mesh-fixation-device
IssueManufacturing defect
TitleLiquiband Fix8 Open Hernia Mesh Fixation Device
ProductLiquiband Fix8 Open Hernia Mesh Fixation Device
Archived0
CategoryGeneral and plastic surgery
Last updated2022-02-14
OrganizationMedical devices
Recall classType I

Overview

  • Recalling FirmMedical devices
  • Risk LevelType I
Official Agency Alert