Home/Recalls/CANADA-59842
Health CanadaType I

HEMOSPRAY ENDOSCOPIC HEMOSTAT (2019-07-24)

Published: July 30, 2019Recall ID: 59842Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

HEMOSPRAY ENDOSCOPIC HEMOSTAT (2019-07-24)

Additional Source Details

FieldValue
N I D59842
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/hemospray-endoscopic-hemostat-2019-07-24
IssueMedical devices
Title HEMOSPRAY ENDOSCOPIC HEMOSTAT (2019-07-24)
Archived0
CategoryMedical devices
Last updated2019-07-30
OrganizationMedical devices
Recall classType I

Overview

  • Recalling FirmMedical devices
  • Risk LevelType I
Official Agency Alert