Nasal Alar Spo2 Sensor (2019-05-08)

Nasal Alar SpO2 Sensor Recall A Nasal Alar SpO2 Sensor used to measure oxygen levels in the blood is being recalled across Canada. The device was distributed starting in 2019 and is being recalled due to safety concerns related to its medical device classification. This recall affects all units of this sensor that were distributed in Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2019-05-24
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/832bd8f9-91aa-43c1-84c3-33aef8f54650