Philips is halting sales of its recalled sleep apnea machines in the US after finding they were pumping foam particles into users’ airways. In its earnings report on Monday, the company says it will not sell new CPAP or BiPAP devices in the US until it meets the requirements outlined by the Food and Drug Administration.
Philips first issued a recall on its sleep apnea machines in 2021 over “potential health risks.” The recall includes devices made between 2009 and April 21st, 2021, and stems from a polyester-based polyurethane foam Philips included in the machines to minimize sound and vibration. As noted by Philips, that foam “can break down,” leading the person using the device to breathe it in or swallow it, resulting in potential…
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