Home/Recalls/CANADA-57848
Health CanadaType II

LENTIS IOLs (2017-09-29)

Published: November 24, 2017Recall ID: 57848Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

LENTIS IOLs (2017-09-29)

Additional Source Details

FieldValue
N I D57848
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/lentis-iols-2017-09-29
IssueMedical devices
Title LENTIS IOLs (2017-09-29)
Archived1
CategoryMedical devices
Last updated2017-11-24
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert