(October 9, 2023, 12:48 PM EDT) -- WASHINGTON, D.C. — The U.S. Food and Drug Administration voiced its dissatisfaction with the process for the recall of continuous positive air pressure (CPAP) devices, bi-level positive air pressure (Bi-PAP) devices and ventilators made by Philips Respironics and announced the launch of a new website “to ensure consumers have the latest information on the Philips' recall.”...