(February 5, 2024, 1:49 PM EST) -- SILVER SPRING, Md. — The U.S. Food and Drug Administration released an update on medical device reports (MDRs) associated with the alleged breakdown of polyester-based polyurethane (PE-PUR) foam used in continuous positive air pressure (CPAP) devices, bi-level positive air pressure (Bi-PAP) devices and ventilators made by Philips Respironics, noting that 111 additional deaths have been reported....