Philips CPAP and Respiratory Device Class Action Information

 

Bob Buckingham Law is planning to commence a national class action on behalf of all persons in Canada who used a Philips CPAP machine, BIPAP machine or mechanical ventilator which are currently subject to a recall by the company.  The complete list of all affected devices can be found here

 

On June 14, 2021, Philips Respironics issued a recall notice in the US for approximately 35 models of its Respiratory Devices that were manufactured with a Polyester-Based Polyurethane (PE-PUR) sound abatement foam. Exposure to the PE-PUR foam can have adverse health effects including, but not limited to, increased cancer risk, respiratory damage, asthma, nausea, vomiting, and headache.

 

It is alleged that Philips Respironics negligently designed and manufactured the Respiratory Devices and failed to warn users of the health risks associated with use of the Respiratory Devices, while assuring users of the safety of its products.

If you believe you use(d) one of the recalled devices, please complete the Class Action Registration Form below.

 

To view the Statement of Claim please click here.

 

 

 
Class Action Registration Form