Home/Recalls/CANADA-63862
Health CanadaType II

Interstim Percutaneous Extension

Published: January 24, 2022Recall ID: 63862Category: generalCountry: Canada

Reason for Recall / Hazard

Increased risk or new adverse events

Product Description & Identification

Interstim Percutaneous Extension

Additional Source Details

FieldValue
N I D63862
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/interstim-percutaneous-extension
IssueIncreased risk or new adverse events
TitleInterstim Percutaneous Extension
ProductInterstim Percutaneous Extension
Archived0
CategoryGastroenterology and urology
Last updated2022-01-24
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert