Home/Recalls/CANADA-59693
Health CanadaType II

BriteBlade Pro Fiber Optic System (2019-09-12)

Published: October 11, 2019Recall ID: 59693Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

BriteBlade Pro Fiber Optic System (2019-09-12)

Additional Source Details

FieldValue
N I D59693
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/briteblade-pro-fiber-optic-system-2019-09-12
IssueMedical devices
Title BriteBlade Pro Fiber Optic System (2019-09-12)
Archived0
CategoryMedical devices
Last updated2019-10-11
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert