Nellcor Spo2 Forehead

Nellcor SpO2 Forehead Recall Summary Nellcor SpO2 Forehead sensors are being recalled across Canada because they may provide inaccurate oxygen level readings. The sensors are used to monitor blood oxygen saturation in patients during medical procedures and hospitalization. This recall affects all Nellcor SpO2 Forehead sensors distributed in Canada.

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-01-18

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/9a5beae7-0df3-40df-9ab8-c423846e274a