Home/Recalls/CANADA-81485
Health CanadaType II

Aesculap unlicenced medical devices

Published: January 15, 2026Recall ID: 81485Category: generalCountry: Canada

Reason for Recall / Hazard

Unauthorised device

Product Description & Identification

Aesculap unlicenced medical devices

Additional Source Details

FieldValue
N I D81485
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/aesculap-unlicenced-medical-devices
IssueUnauthorised device
TitleAesculap unlicenced medical devices
ProductAesculap unlicenced medical devices
Archived0
CategoryGeneral and plastic surgery - Gastroenterology and urology - Orthopaedics - Neurology - Ophthalmology - Obstetrics and gynaecology
Last updated2026-01-15
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert