Home/Recalls/CANADA-58099
Health CanadaType III

Pro-Vent Plus, Anaerobic Pulsator Plus, Pulsator Liquid Heparin, and Dry Pulsato...

Published: July 19, 2018Recall ID: 58099Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Pro-Vent Plus, Anaerobic Pulsator Plus, Pulsator Liquid Heparin, and Dry Pulsator Plus Arterial Blood Gas Sampling Kit (2018-06-26)

Additional Source Details

FieldValue
N I D58099
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/pro-vent-plus-anaerobic-pulsator-plus-pulsator-liquid-heparin-and-dry-pulsator-plus
IssueMedical devices
Title Pro-Vent Plus, Anaerobic Pulsator Plus, Pulsator Liquid Heparin, and Dry Pulsator Plus Arterial Blood Gas Sampling Kit (2018-06-26)
Archived0
CategoryMedical devices
Last updated2018-07-19
OrganizationMedical devices
Recall classType III

Overview

  • Recalling FirmMedical devices
  • Risk LevelType III
Official Agency Alert