Home/Recalls/CANADA-81630
Health CanadaType II

Celon ProBreath and Celon ProSleep Applicators

Published: February 20, 2026Recall ID: 81630Category: generalCountry: Canada

Reason for Recall / Hazard

Labelling and packaging

Product Description & Identification

Celon ProBreath and Celon ProSleep Applicators

Additional Source Details

FieldValue
N I D81630
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/celon-probreath-and-celon-prosleep-applicators
IssueLabelling and packaging
TitleCelon ProBreath and Celon ProSleep Applicators
ProductCelon ProBreath and Celon ProSleep Applicators
Archived0
CategoryGeneral and plastic surgery
Last updated2026-02-20
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert