Home/Recalls/CANADA-82136
Health CanadaType II

CRE™ Wireguided and CRE PRO™ Wireguided Balloon Dilation Catheters

Published: May 29, 2026Recall ID: 82136Category: generalCountry: Canada

Reason for Recall / Hazard

Sterility

Product Description & Identification

CRE™ Wireguided and CRE PRO™ Wireguided Balloon Dilation Catheters

Additional Source Details

FieldValue
N I D82136
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/cretm-wireguided-and-cre-protm-wireguided-balloon-dilation-catheters
IssueSterility
TitleCRE™ Wireguided and CRE PRO™ Wireguided Balloon Dilation Catheters
ProductCRE™ Wireguided and CRE PRO™ Wireguided Balloon Dilation Catheters
Archived0
CategoryGeneral and plastic surgery
Last updated2026-05-29
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert