Home/Recalls/CANADA-59823
Health CanadaType II

DELFIA/AutoDELFIA P1GF Kit (2019-08-07)

Published: August 16, 2019Recall ID: 59823Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

DELFIA/AutoDELFIA P1GF Kit (2019-08-07)

Additional Source Details

FieldValue
N I D59823
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/delfiaautodelfia-p1gf-kit-2019-08-07
IssueMedical devices
Title DELFIA/AutoDELFIA P1GF Kit (2019-08-07)
Archived0
CategoryMedical devices
Last updated2019-08-16
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert