Home/Recalls/CANADA-75561
Health CanadaType I

IOMAX Cortical Module

Published: May 24, 2024Recall ID: 75561Category: generalCountry: Canada

Reason for Recall / Hazard

Performance

Product Description & Identification

IOMAX Cortical Module

Additional Source Details

FieldValue
N I D75561
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/iomax-cortical-module-0
IssuePerformance
TitleIOMAX Cortical Module
ProductIOMAX Cortical Module
Archived0
CategoryNeurology
Last updated2024-05-24
OrganizationMedical devices
Recall classType I

Overview

  • Recalling FirmMedical devices
  • Risk LevelType I
Official Agency Alert