Home/Recalls/CANADA-63903
Health CanadaType II

Biolox Delta

Published: February 8, 2022Recall ID: 63903Category: generalCountry: Canada

Reason for Recall / Hazard

Labelling and packaging

Product Description & Identification

Biolox Delta

Additional Source Details

FieldValue
N I D63903
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/biolox-delta
IssueLabelling and packaging
TitleBiolox Delta
ProductBiolox Delta
Archived0
CategoryOrthopaedics
Last updated2022-02-08
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert