Home/Recalls/CANADA-58101
Health CanadaType III

Lysercell WDF (2018-06-25)

Published: July 19, 2018Recall ID: 58101Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Lysercell WDF (2018-06-25)

Additional Source Details

FieldValue
N I D58101
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/lysercell-wdf-2018-06-25
IssueMedical devices
Title Lysercell WDF (2018-06-25)
Archived0
CategoryMedical devices
Last updated2018-07-19
OrganizationMedical devices
Recall classType III

Overview

  • Recalling FirmMedical devices
  • Risk LevelType III
Official Agency Alert