Recalled Philips Ventilators, BiPAP Machines, and CPAP Machines
Nov 20, 2024 · In June 2021, Philips Respironics (Philips) recalled certain ventilators, bi-level positive airway pressure (also known as Bilevel PAP, BiPAP, or BPAP) machines, and …
Medical Device Recall Information - Philips Respironics Sleep and ...
In June 2021, after discovering a potential health risk related to a part in certain CPAP, BiPAP and Mechanical Ventilator devices, Philips issued a voluntary Field Safety Notice (outside U.S.) / …
CPAP Recalls: What You Need To Know - Sleep Foundation
Jul 9, 2025 · Recalls of a popular brand of CPAP machine have affected millions of Americans. Learn about the Philips recalls, concerns regarding replacements, and lawsuits.
FDA Issues New Recall Alert For ResMed CPAP Devices: Here's …
Jun 3, 2024 · In 2022, Philips’ CPAP machines also faced a Class I device recall from the FDA due to similar magnet interference concerns. Patients should have received information from …
Recalled Sleep Apnea Machines Linked to Over 500 Deaths
Feb 7, 2024 · Last week, the U.S. Food and Drug Administration (FDA) announced that previously recalled sleep apnea machines have now been tied to the deaths of over 550 people.
CPAP Machine Recalls: What You Need to Know
Apr 11, 2024 · Several CPAP machines have been recalled. We explain reasons for recalls, how to find out whether your CPAP machine is recalled, and what to do next.
FDA updates on serious Philips CPAP, BiPAP device recall
Sep 15, 2025 · For years, the unit grappled with a significant respiratory device recall that knocked it out of the market at one point. The FDA issued a notice to warn of the latest recall, …
Philips CPAP Recall: Updates & FDA Safety News - Drugwatch
Mar 7, 2025 · Learn the latest on the Philips CPAP machine recalls, dangers to their users, what to do if you’re affected and financial settlements from the company.
FDA Updates Injury, Death Reports from Ventilator Inoperative …
Aug 5, 2025 · This week, the Food and Drug Administration (FDA) issued an update to its 2024 recall notice of Philips BiPAP V30, A30, and A40 ventilators related to the risk for a failure in …
Information for patients and caregivers | Philips
Registration for affected CPAP and BiPAP devices in the US and Canada closed on December 31, 2024. As of July 1, 2025, the US Patient Portal has reduced operations to a limited set of …