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Philips CPAP, BiPAP Devices Foam Poses Health Risks Complaint

July 1, 2021

CPAP, BiPAP, and mechanical ventilator devices are used to treat sleep apnea. Unfortunately, the complaint for this class action alleges that certain devices from Koninklijke Philips NV, Philips North America, LLC, and Philips RS North America, LLC were made with an objectionable polyester-based polyurethane sound abatement foam (PE-PUR foam) that can degrade into particles that can be ingested or inhaled.

Case Event File: Philips CPAP, BiPAP Devices Foam Poses Health Risks Complaint

Related to: Philips CPAP, BiPAP Devices Foam Poses Health Risks Class Action