Home/Recalls/CANADA-59788
Health CanadaType III

MOBILETT Elara Max (2019-06-26)

Published: July 19, 2019Recall ID: 59788Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

MOBILETT Elara Max (2019-06-26)

Additional Source Details

FieldValue
N I D59788
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/mobilett-elara-max-2019-06-26
IssueMedical devices
Title MOBILETT Elara Max (2019-06-26)
Archived0
CategoryMedical devices
Last updated2019-07-19
OrganizationMedical devices
Recall classType III

Overview

  • Recalling FirmMedical devices
  • Risk LevelType III
Official Agency Alert