Home/Recalls/CANADA-61866
Health CanadaType II

K-ACT Kaolin ACT Tubes (2020-11-09)

Published: November 27, 2020Recall ID: 61866Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

K-ACT Kaolin ACT Tubes (2020-11-09)

Additional Source Details

FieldValue
N I D61866
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/k-act-kaolin-act-tubes-2020-11-09
IssueMedical devices
Title K-ACT Kaolin ACT Tubes (2020-11-09)
Archived0
CategoryMedical devices
Last updated2020-11-27
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert