Fabian Hfo, +ncpap Evolution, Therapy Evolution (2021-04-22)

Recall Summary Philips is recalling certain Respironics sleep apnea and ventilation devices (Fabian HFO, nCPAP evolution, and Therapy evolution models from 2021) distributed across Canada due to potential issues related to COVID-related contamination concerns. This is a Class I recall, meaning the devices could cause serious health problems or death. The recall affects patients in Canada who are using these specific respiratory therapy devices.

Reason

COVID - Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2021-05-26

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/6733f11e-c50f-452e-8211-652f8f298ee5