Philips Faces Class Action for Unsafe and Defective Sleep Apnea Machines and Ventilators

Schubert Jonckheer & Kolbe LLP is investigating the recent recall of certain sleep apnea machines and ventilators made by Philips.

On June 14, 2021, Philips issued a recall for many of its Bi-Level Positive Airway Pressure (Bi-Level PAP), Continuous Positive Airway Pressure (CPAP), and mechanical ventilator devices because these products contain foam that could put users at risk of cancer and other serious health issues. The defect is related to polyester-based polyurethane (PE-PUR) sound abatement foam in the devices, which can degrade and cause harmful effects during cleaning or when exposed to high heat and humidity. The potential risks of exposure include headaches, dizziness, irritation (skin, eyes, nose, and respiratory tract), inflammation, respiratory issues, nausea, vomiting, and possible toxic and carcinogenic effects.

The recall does not immediately provide users with new, defect-free, machines, money for replacement equipment, or parts or other methods to repair their current devices.

If you purchased any of the recalled Philips products pictured below and would like to learn more about your legal rights — or would like to participate in a class action lawsuit —please complete the form below for a free legal consultation.