Home/Recalls/CANADA-51012
Health CanadaType III

Beckman Coulter Cell Preparation System FP1000 (2013-11-25)

Published: January 13, 2014Recall ID: 51012Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Beckman Coulter Cell Preparation System FP1000 (2013-11-25)

Additional Source Details

FieldValue
N I D51012
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/beckman-coulter-cell-preparation-system-fp1000-2013-11-25
IssueMedical devices
Title Beckman Coulter Cell Preparation System FP1000 (2013-11-25)
Archived1
CategoryMedical devices
Last updated2014-01-13
OrganizationMedical devices
Recall classType III

Overview

  • Recalling FirmMedical devices
  • Risk LevelType III
Official Agency Alert