Home/Recalls/CANADA-55059
Health CanadaType II

Unlicensed Dynarex Products (2016-02-15)

Published: April 22, 2016Recall ID: 55059Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Unlicensed Dynarex Products (2016-02-15)

Additional Source Details

FieldValue
N I D55059
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/unlicensed-dynarex-products-2016-02-15
IssueMedical devices
Title Unlicensed Dynarex Products (2016-02-15)
Archived1
CategoryMedical devices
Last updated2016-04-22
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert