Home/Recalls/CANADA-50787
Health CanadaType I

Remipack (2013-12-12)

Published: February 3, 2014Recall ID: 50787Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Remipack (2013-12-12)

Additional Source Details

FieldValue
N I D50787
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/remipack-2013-12-12
IssueMedical devices
Title Remipack (2013-12-12)
Archived1
CategoryMedical devices
Last updated2014-02-03
OrganizationMedical devices
Recall classType I

Overview

  • Recalling FirmMedical devices
  • Risk LevelType I
Official Agency Alert