Home/Recalls/CANADA-51891
Health CanadaType III

Kamra Corneal Inlay ACI 7000 (2013-11-08)

Published: June 12, 2014Recall ID: 51891Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Kamra Corneal Inlay ACI 7000 (2013-11-08)

Additional Source Details

FieldValue
N I D51891
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/kamra-corneal-inlay-aci-7000-2013-11-08
IssueMedical devices
Title Kamra Corneal Inlay ACI 7000 (2013-11-08)
Archived1
CategoryMedical devices
Last updated2014-06-12
OrganizationMedical devices
Recall classType III

Overview

  • Recalling FirmMedical devices
  • Risk LevelType III
Official Agency Alert