![]() ![]() ![]() Furthermore, the foam may off-gas certain chemicals. These particles can then enter the device’s air pathway and be ingested or inhaled by the user. Based on reports and testing, Philips determined the PE-PUR foam could degrade into particles. Philips first publicized the adverse, foam-related effects of its CPAP and Bi-Level PAP devices in its first-quarter 2021 company report. The recalled devices include those in the first-generation DreamStation product family. This component can disintegrate or outgas, causing users to inhale and/or ingest toxic and possibly carcinogenic substances. The recall provides potential health risks the company identified in their devices’ polyester-based polyurethane (PE-PUR) sound abatement foam component. On June 14, 2021, Philips announced a voluntary recall for various Philips Bi-Level Positive Airway Pressure (Bi-Level PAP), Continuous Positive Airway Pressure (CPAP), and mechanical ventilator devices. ![]()
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