Home/Recalls/CANADA-59888
Health CanadaType III

Cobas IT Middleware (2019-07-26)

Published: August 16, 2019Recall ID: 59888Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Cobas IT Middleware (2019-07-26)

Additional Source Details

FieldValue
N I D59888
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/cobas-it-middleware-2019-07-26
IssueMedical devices
Title Cobas IT Middleware (2019-07-26)
Archived0
CategoryMedical devices
Last updated2019-08-16
OrganizationMedical devices
Recall classType III

Overview

  • Recalling FirmMedical devices
  • Risk LevelType III
Official Agency Alert