Home/Recalls/CANADA-74195
Health CanadaType II

Pentacam® AXL Wave and Myopia Master®

Published: August 24, 2023Recall ID: 74195Category: generalCountry: Canada

Reason for Recall / Hazard

Performance

Product Description & Identification

Pentacam® AXL Wave and Myopia Master®

Additional Source Details

FieldValue
N I D74195
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/pentacamr-axl-wave-and-myopia-masterr
IssuePerformance
TitlePentacam® AXL Wave and Myopia Master®
ProductPentacam® AXL Wave and Myopia Master®
Archived0
CategoryOphthalmology
Last updated2023-08-24
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert