Home/Recalls/CANADA-78073
Health CanadaType II

Hollow Fiber Hemodialyzers

Published: September 16, 2025Recall ID: 78073Category: generalCountry: Canada

Reason for Recall / Hazard

Labelling and packaging

Product Description & Identification

Hollow Fiber Hemodialyzers

Additional Source Details

FieldValue
N I D78073
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/hollow-fiber-hemodialyzers
IssueLabelling and packaging
TitleHollow Fiber Hemodialyzers
ProductHollow Fiber Hemodialyzers
Archived0
CategoryGastroenterology and urology
Last updated2025-09-16
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert