Home/Recalls/CANADA-63615
Health CanadaType II

ALOKA ARIETTA 850

Published: November 19, 2021Recall ID: 63615Category: generalCountry: Canada

Reason for Recall / Hazard

Inaccurate test or measurement results

Product Description & Identification

ALOKA ARIETTA 850

Additional Source Details

FieldValue
N I D63615
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/aloka-arietta-850
IssueInaccurate test or measurement results
TitleALOKA ARIETTA 850
ProductALOKA ARIETTA 850
Archived0
CategoryObstetrics and gynaecology
Last updated2021-11-19
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert