Home/Recalls/CANADA-78470
Health CanadaType II

Single Use Ligating Device PolyLoop™

Published: November 7, 2025Recall ID: 78470Category: generalCountry: Canada

Reason for Recall / Hazard

Performance

Product Description & Identification

Single Use Ligating Device PolyLoop™

Additional Source Details

FieldValue
N I D78470
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/single-use-ligating-device-polylooptm
IssuePerformance
TitleSingle Use Ligating Device PolyLoop™
ProductSingle Use Ligating Device PolyLoop™
Archived0
CategoryGastroenterology and urology
Last updated2025-11-07
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert