Home/Recalls/CANADA-57893
Health CanadaType III

ARJOHUNTLEIGH MAXI MOVE HANDSET (2016-05-20)

Published: November 30, 2017Recall ID: 57893Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

ARJOHUNTLEIGH MAXI MOVE HANDSET (2016-05-20)

Additional Source Details

FieldValue
N I D57893
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/arjohuntleigh-maxi-move-handset-2016-05-20
IssueMedical devices
Title ARJOHUNTLEIGH MAXI MOVE HANDSET (2016-05-20)
Archived1
CategoryMedical devices
Last updated2017-11-30
OrganizationMedical devices
Recall classType III

Overview

  • Recalling FirmMedical devices
  • Risk LevelType III
Official Agency Alert