Home/Recalls/CANADA-52162
Health CanadaType III

ABX PENTRA Magnesium RTU (2014-09-26)

Published: October 10, 2014Recall ID: 52162Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

ABX PENTRA Magnesium RTU (2014-09-26)

Additional Source Details

FieldValue
N I D52162
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/abx-pentra-magnesium-rtu-2014-09-26
IssueMedical devices
Title ABX PENTRA Magnesium RTU (2014-09-26)
Archived1
CategoryMedical devices
Last updated2014-10-10
OrganizationMedical devices
Recall classType III

Overview

  • Recalling FirmMedical devices
  • Risk LevelType III
Official Agency Alert