Home/Recalls/CANADA-50113
Health CanadaType II

Torflex Transseptal Guiding Sheath (2013-09-24)

Published: October 31, 2013Recall ID: 50113Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Torflex Transseptal Guiding Sheath (2013-09-24)

Additional Source Details

FieldValue
N I D50113
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/torflex-transseptal-guiding-sheath-2013-09-24
IssueMedical devices
Title Torflex Transseptal Guiding Sheath (2013-09-24)
Archived1
CategoryMedical devices
Last updated2013-10-31
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert