Home/Recalls/CANADA-50785
Health CanadaType II

Kodak Directview DR 7500 System and DRX-Evolution Systems (2013-12-02)

Published: February 3, 2014Recall ID: 50785Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Kodak Directview DR 7500 System and DRX-Evolution Systems (2013-12-02)

Additional Source Details

FieldValue
N I D50785
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/kodak-directview-dr-7500-system-and-drx-evolution-systems-2013-12-02
IssueMedical devices
Title Kodak Directview DR 7500 System and DRX-Evolution Systems (2013-12-02)
Archived1
CategoryMedical devices
Last updated2014-02-03
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert