Home/Recalls/CANADA-62113
Health CanadaType II

PRECISE PRO RX NITINOL STENT SYSTEM (2021-02-16)

Published: March 4, 2021Recall ID: 62113Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

PRECISE PRO RX NITINOL STENT SYSTEM (2021-02-16)

Additional Source Details

FieldValue
N I D62113
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/precise-pro-rx-nitinol-stent-system-2021-02-16
IssueMedical devices
Title PRECISE PRO RX NITINOL STENT SYSTEM (2021-02-16)
Archived0
CategoryMedical devices
Last updated2021-03-04
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert