Philips Bipap And Humidifiers

Philips BiPAP and Humidifiers Recall Philips BiPAP and humidifier devices are being recalled across Canada because they may not be sterile as required. This is a Class I recall, meaning there is a serious potential health risk associated with the products. The affected devices were distributed throughout Canada.

Product

Philips BiPAP and Humidifiers

Reason

Sterility

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2023-07-10

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/b15e1f03-0a2b-46a7-9fbb-59c9d77cd8f9