F&p Sleepstyle Cpap Device (2018-03-14)

F&P SleepStyle CPAP Device Recall Fisher & Paykel's SleepStyle CPAP devices are being recalled across Canada due to a medical device issue. This recall is classified as Class I, which is the most serious type. The affected devices were distributed nationwide in Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2018-04-03

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/1a955127-9009-43b9-ab19-ba2268790520