Home/Recalls/CANADA-57080
Health CanadaType III

BIOPHEN ARIXTRA CONTROL PLASMA (2017-09-01)

Published: September 26, 2017Recall ID: 57080Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

BIOPHEN ARIXTRA CONTROL PLASMA (2017-09-01)

Additional Source Details

FieldValue
N I D57080
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/biophen-arixtra-control-plasma-2017-09-01
IssueMedical devices
Title BIOPHEN ARIXTRA CONTROL PLASMA (2017-09-01)
Archived1
CategoryMedical devices
Last updated2017-09-26
OrganizationMedical devices
Recall classType III

Overview

  • Recalling FirmMedical devices
  • Risk LevelType III
Official Agency Alert