Home/Recalls/CANADA-55993
Health CanadaType II

OMNILAB V.12.0 - LABORATORY INFORMATION SYSTEM (2016-08-11)

Published: August 26, 2016Recall ID: 55993Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

OMNILAB V.12.0 - LABORATORY INFORMATION SYSTEM (2016-08-11)

Additional Source Details

FieldValue
N I D55993
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/omnilab-v120-laboratory-information-system-2016-08-11
IssueMedical devices
Title OMNILAB V.12.0 - LABORATORY INFORMATION SYSTEM (2016-08-11)
Archived1
CategoryMedical devices
Last updated2016-08-26
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert