Home/Recalls/CANADA-51910
Health CanadaType II

Kodak Directview DR 9000 System (2014-06-02)

Published: June 18, 2014Recall ID: 51910Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Kodak Directview DR 9000 System (2014-06-02)

Additional Source Details

FieldValue
N I D51910
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/kodak-directview-dr-9000-system-2014-06-02
IssueMedical devices
Title Kodak Directview DR 9000 System (2014-06-02)
Archived1
CategoryMedical devices
Last updated2014-06-18
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert