Home/Recalls/CANADA-63828
Health CanadaType II

Bd Veritor Plus Analyzer

Published: January 17, 2022Recall ID: 63828Category: generalCountry: Canada

Reason for Recall / Hazard

Increased risk or new adverse events

Product Description & Identification

Bd Veritor Plus Analyzer

Additional Source Details

FieldValue
N I D63828
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/bd-veritor-plus-analyzer
IssueIncreased risk or new adverse events
TitleBd Veritor Plus Analyzer
ProductBd Veritor Plus Analyzer
Archived0
CategoryMedical devices
Last updated2022-01-17
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert