Home/Recalls/CANADA-77630
Health CanadaType II

VersaCross™ Access Solution, TorFlex™ Transseptal Guiding Sheath and VersaCross™...

Published: June 19, 2025Recall ID: 77630Category: generalCountry: Canada

Reason for Recall / Hazard

Sterility

Product Description & Identification

VersaCross™ Access Solution, TorFlex™ Transseptal Guiding Sheath and VersaCross™ Transseptal Sheath

Additional Source Details

FieldValue
N I D77630
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/versacrosstm-access-solution-torflextm-transseptal-guiding-sheath-and-versacrosstm
IssueSterility
TitleVersaCross™ Access Solution, TorFlex™ Transseptal Guiding Sheath and VersaCross™ Transseptal Sheath
ProductVersaCross™ Access Solution, TorFlex™ Transseptal Guiding Sheath and VersaCross™ Transseptal Sheath
Archived0
CategoryCardiovascular
Last updated2025-06-19
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert