Home/Recalls/CANADA-58478
Health CanadaType II

Kodak DirectView DR 7500 System (2018-10-28)

Published: November 15, 2018Recall ID: 58478Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Kodak DirectView DR 7500 System (2018-10-28)

Additional Source Details

FieldValue
N I D58478
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/kodak-directview-dr-7500-system-2018-10-28
IssueMedical devices
Title Kodak DirectView DR 7500 System (2018-10-28)
Archived0
CategoryMedical devices
Last updated2018-11-15
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert