![]() The PE-PUR sound abatement foam can degrade into small particles which could enter the device’s air pathway and be ingested or inhaled by the user. In addition, the class action lawsuit filed alleges that Philips timed the recall to coincide with the launch of new products, resulting in customers purchasing a newer model to resolve their issues. The lawsuit alleges that Philips was aware of the material risks associated with CPAP and Bi-Level PAP machines long before the voluntary recall. ![]() The majority of the affected devices within the advised 5-year service life are in the first-generation DreamStation product family.Ī class action lawsuit was filed in Massachusetts on June 30 by the national plaintiffs’ law firm Berger Montague. The recall was the result of “identified potential health risks related to the polyester-based polyurethane (PE-PUR) sound abatement foam component of these devices.” This observation was originally made in April 2021 in the Philips Q1 2021 Quarterly Report. ![]() On June 14, 2021, Royal Philips (NYSE: PHG, AEX: PHIA) issued a voluntary recall notification for specific Philips Continuous Positive Airway Pressure (CPAP), Bi-Level Positive Airway Pressure (Bi-Level PAP), and mechanical ventilator devices.
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