Home/Recalls/CANADA-56079
Health CanadaType III

PreciPath U Plus Control

Published: November 18, 2016Recall ID: 56079Category: generalCountry: Canada

Product Description & Identification

PreciPath U Plus Control

Additional Source Details

FieldValue
N I D56079
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/precipath-u-plus-control
Title PreciPath U Plus Control
Archived1
CategoryMedical devices
Last updated2016-11-18
OrganizationMedical devices
Recall classType III

Overview

  • Recalling FirmMedical devices
  • Risk LevelType III
Official Agency Alert