Home/Recalls/CANADA-55351
Health CanadaType II

PRECISE PRO RX NITINOL STENT SYSTEM (2016-05-06)

Published: May 24, 2016Recall ID: 55351Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

PRECISE PRO RX NITINOL STENT SYSTEM (2016-05-06)

Additional Source Details

FieldValue
N I D55351
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/precise-pro-rx-nitinol-stent-system-2016-05-06
IssueMedical devices
Title PRECISE PRO RX NITINOL STENT SYSTEM (2016-05-06)
Archived1
CategoryMedical devices
Last updated2016-05-24
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert