Home/Recalls/CANADA-51255
Health CanadaType II

Dermalight 80 Psoracomb (2013-04-08)

Published: March 20, 2014Recall ID: 51255Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Dermalight 80 Psoracomb (2013-04-08)

Additional Source Details

FieldValue
N I D51255
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/dermalight-80-psoracomb-2013-04-08
IssueMedical devices
Title Dermalight 80 Psoracomb (2013-04-08)
Archived1
CategoryMedical devices
Last updated2014-03-20
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert