Home/Recalls/CANADA-51702
Health CanadaType II

Kodak Directview DR 7500 system (2014-07-11)

Published: July 22, 2014Recall ID: 51702Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Kodak Directview DR 7500 system (2014-07-11)

Additional Source Details

FieldValue
N I D51702
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/kodak-directview-dr-7500-system-2014-07-11
IssueMedical devices
Title Kodak Directview DR 7500 system (2014-07-11)
Archived1
CategoryMedical devices
Last updated2014-07-22
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert