Home/Recalls/CANADA-58258
Health CanadaType II

Allura Xper FD10, FD20, FD10/10, and FD20/10 (2018-06-12)

Published: August 17, 2018Recall ID: 58258Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Allura Xper FD10, FD20, FD10/10, and FD20/10 (2018-06-12)

Additional Source Details

FieldValue
N I D58258
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/allura-xper-fd10-fd20-fd1010-and-fd2010-2018-06-12
IssueMedical devices
Title Allura Xper FD10, FD20, FD10/10, and FD20/10 (2018-06-12)
Archived0
CategoryMedical devices
Last updated2018-08-17
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert