Home/Recalls/CANADA-57814
Health CanadaType II

PRESOURCE STERILE DIEP BUNDLE PASQUA PK (2017-11-15)

Published: December 8, 2017Recall ID: 57814Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

PRESOURCE STERILE DIEP BUNDLE PASQUA PK (2017-11-15)

Additional Source Details

FieldValue
N I D57814
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/presource-sterile-diep-bundle-pasqua-pk-2017-11-15
IssueMedical devices
Title PRESOURCE STERILE DIEP BUNDLE PASQUA PK (2017-11-15)
Archived1
CategoryMedical devices
Last updated2017-12-08
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert