Home/Recalls/CANADA-52631
Health CanadaType II

Actiwatch Spectrum Plus (2014-06-02)

Published: January 21, 2015Recall ID: 52631Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Actiwatch Spectrum Plus (2014-06-02)

Additional Source Details

FieldValue
N I D52631
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/actiwatch-spectrum-plus-2014-06-02
IssueMedical devices
Title Actiwatch Spectrum Plus (2014-06-02)
Archived1
CategoryMedical devices
Last updated2015-01-21
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert