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Philips device recall

Philips device recall

Updated: July 8th, 2021, at 9:00 a.m.

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 devices. 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.

Recalled devices

Types of devices covered by the recall

Recalled devices

Available options

Solutions to help you

Available options

Medical follow-up

Get an appointment to follow-up on your treatment

Medical follow-up

Sign-up for the Philips registry

Register your device to the Philips recall registry

Sign-up for the Philips registry

Notice of availability

Be informed about the availability of devices from other suppliers

Notice of availability

Frequently asked questions

Find answers to your questions

Frequently asked questions
Decision Support Tool

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).