Celon Probreath And Celon Prosleep Applicators

Celon ProBreath and Celon ProSleep Applicators are being recalled across Canada due to labelling and packaging issues. This is classified as a Class I recall, the most serious type. The recall affects these products wherever they were distributed in Canada.

Product
Celon ProBreath and Celon ProSleep Applicators
Reason
Labelling or packaging defect
Classification
Class II
Category
medical device recall
Country
Canada
Agency
HC-DEVICES
Recall date
2026-02-20
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/afaab511-e3a6-4b87-84c9-a2496311a779