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Philips device recall

Updated: July 31, 2023, 9:00 a.m.

Philips device recall

For the lastest updates on the Philips recall, visit our dedicated section below.

On June 14, 2021, sleep apnea device manufacturer Philips announced that it is recalling several of its models currently on the market. This recall, confirmed by Health Canada on June 23, 2021, is taking place due to the health risks associated with the use of the affected device. An update from Health Canada was provided on July 27, 2022.

Although Biron is not responsible for this recall, every effort is being made to find ways to assist and support our customers. Rest assured that we are monitoring the situation very closely and remain fully committed to communicating with our customers on an ongoing basis regarding this issue.

Update of the recall

Stay informed about the latest news related to the Philips recall

Read the information
Update of the recall

Recalled devices

Types of devices covered by the recall

See the full list
Recalled devices

Available options

Solutions to help you

View the options
Available options

Sign-up for the Philips registry

Register your device to the Philips recall registry

Consult the procedure
Sign-up for the Philips registry

Replacement process

Find out how to exchange a recalled CPAP machine

Exchange your device
Replacement process

Frequently asked questions

Find answers to your questions

Visit the FAQ page
Frequently asked questions
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Decision Support Tool

The recommendations in this section of Biron’s website are issued by the Centre hospitalier universitaire de Montréal (CHUM). This is an excerpt from the information provided by the CHUM. You can view the original and complete version of these recommendations on the website of the CHUM (available in French only).

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