Home/Recalls/CANADA-53151
Health CanadaType III

AccuMAb Plus Bordetella pertussis /parapertussis DFA (2014-03-01)

Published: May 21, 2015Recall ID: 53151Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

AccuMAb Plus Bordetella pertussis /parapertussis DFA (2014-03-01)

Additional Source Details

FieldValue
N I D53151
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/accumab-plus-bordetella-pertussis-parapertussis-dfa-2014-03-01
IssueMedical devices
Title AccuMAb Plus Bordetella pertussis /parapertussis DFA (2014-03-01)
Archived1
CategoryMedical devices
Last updated2015-05-21
OrganizationMedical devices
Recall classType III

Overview

  • Recalling FirmMedical devices
  • Risk LevelType III
Official Agency Alert