Home/Recalls/CANADA-58313
Health CanadaType II

Stimuplex Ultra 360 Insulated Echogenic Needle and Ultraplex 360 Non-Stimulating...

Published: October 19, 2018Recall ID: 58313Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Stimuplex Ultra 360 Insulated Echogenic Needle and Ultraplex 360 Non-Stimulating Echogenic Needle (2018-09-24)

Additional Source Details

FieldValue
N I D58313
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/stimuplex-ultra-360-insulated-echogenic-needle-and-ultraplex-360-non-stimulating
IssueMedical devices
Title Stimuplex Ultra 360 Insulated Echogenic Needle and Ultraplex 360 Non-Stimulating Echogenic Needle (2018-09-24)
Archived0
CategoryMedical devices
Last updated2018-10-19
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert