Home/Recalls/CANADA-52750
Health CanadaType II

ABL800 Flex System-CREA Electrode and Membrane (2014-10-29)

Published: November 26, 2014Recall ID: 52750Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

ABL800 Flex System-CREA Electrode and Membrane (2014-10-29)

Additional Source Details

FieldValue
N I D52750
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/abl800-flex-system-crea-electrode-and-membrane-2014-10-29
IssueMedical devices
Title ABL800 Flex System-CREA Electrode and Membrane (2014-10-29)
Archived1
CategoryMedical devices
Last updated2014-11-26
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert