Philips cpap recall Patient safety is our top priority, and we are committed to supporting our patients, durable medical equipment providers (DMEs), distributors, home 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. Philips Respironics plans to close its Sep 15, 2025 · Philips has agreed to a $1. 1 This includes DreamStation CPAP, Auto CPAP; Dream Station Bi-Level PAP; DreamStation ASV; and DreamStation ST, AVAPS devices. COMPANY ANNOUNCEMENT Philips Issues a Recall Notification* to Mitigate Potential Health Risks Related to the Sound Abatement Foam Component in Certain Sleep and Respiratory Care Devices Aug 15, 2024 · Following the initial recall in June 2021, Philips developed a plan to repair the PE-PUR foam in the recalled CPAP and BiPAP devices with a different, silicone-based foam. Following the issuance of the recall notification/field safety notice* in June 2021, Philips Respironics initiated a global program to remediate the Returning a recalled Philips CPAP machine involves multiple layers of complex steps, from verifying whether your device is under recall to coordinating shipment and, if needed, seeking legal recourse. Jun 14, 2021 · On June 14, Philips issued a recall notification for specific Philips CPAP, bi-level PAP, and mechanical ventilator devices. 8 million CPAP and other breathing devices due to health risks associated with its sound-reducing foam. Philips Respironics will no longer accept new registrations for affected CPAP and BiPAP devices in the US after December 31, 2024. Because of our commitment to transparency, we want you to have the correct information about the legal process. Feb 28, 2025 · Philips Respironics will not accept new registrations for affected CPAP and BiPAP devices in the US after December 31, 2024. Dec 9, 2024 · In 2021, Philips recalled 10. This private Settlement Program is intended to resolve What products were recalled?In June 2021, Philips Respironics initiated a voluntary recall notification for certain CPAP and BiPAP sleep therapy devices and mechanical ventilators to address potential health risks related to the polyester-based polyurethane (PE-PUR) sound abatement foam in these devices. He claims The Philips Dreamstation CPAP device, recalled in 2023, is still being used and could pose a cancer risk to users. Devices authorized for repair and replacement include DreamStation CPAP and BiLevel devices, DreamStation ASV devices, and DreamStation ST/AVAPS devices. Philips acted to protect patient safety by initiating and executing a voluntary recall/field action of significant scale in June 2021. Users and patients should contact Philips for pressure changes or replacement devices and follow the instructions in the Important Product Notice. ) / voluntary recall notification (U. Sep 8, 2022 · A recall was issued on 17 million sleep apnea masks manufactured by Philips that contain magnetic clips. Sep 1, 2023 · We surveyed clinician members of the American Academy of Sleep Medicine to quantify the recall’s impact. When was the recall initiated? On June 14, 2021, Philips initiated a voluntary U. To receive a replacement device or financial payment, please be sure to register your device prior to the end of the year. Nov 7, 2025 · Philips CPAP Recall Lawsuit | 2025 Latest Updates Philips is recalling certain Bi-Level Positive Airway Pressure (Bi-Level PAP) machines, Continuous Positive Airway Pressure (CPAP) devices, and mechanical ventilators over concerns they could increase the risk of cancer and other toxic respiratory effects. The Philips recall covered an estimated 3. Contact and support options for patients impacted by the June 2021 voluntary recall of certain CPAP, BiPAP and mechanical ventilators related to PE-PUR sound abatement foam. Class Action Details The claim concerns sleep and respiratory care devices manufactured, marketed, and sold by the Defendants, particularly Philips Respironics branded Continuous Positive Airway Pressure (CPAP), Bi-Level Positive Airway Pressure (BIPAP), and Mechanical Ventilators. For patients using life-sustaining mechanical ventilator devices: DO NOT discontinue or alter Jun 20, 2024 · The DreamStation CPAP is among the devices involved in Philips’ respiratory devices recall. Jan 10, 2025 · Philips Respironics has recalled millions of ventilators, BiPAP, and CPAP machines. The recall was initiated due to the degradation of Sep 12, 2024 · Philips has announced a recall on several of its CPAP and BiPAP machines due to cancer risks of foam degradation. Voluntary recall of CPAP and Bi-Level PAP Devices and Mechanical Ventilators (sound abatement foam) Initiated June 2021 The foam that is used in some devices to reduce sound and vibration showed signs of degradation (damage) and chemical emissions. Patient safety is our top Apr 29, 2024 · Philips announced a recall for millions of their Bi-Level Positive Airway Pressure (Bi-Level PAP), Continuous Positive Airway Pressure (CPAP), and mechanical ventilator devices in 2021. We continue to work with independent partners to conduct extensive testing and analysis of results on affected Apr 29, 2022 · Sleep apnea sufferers all over the world are wondering what’s going on with their CPAP machines. You can follow the FDA Safety Communication regarding Philips CPAP lawsuit updates and developments here: Sep 5, 2024 · Do you qualify for a Philips CPAP Lawsuit? If you used a Philips CPAP machine included in the recall and suffered health problems like lung cancer, respiratory issues, or possible exposure to toxic chemicals, speak to a lawyer today! Especially if your CPAP machine is a Philips Respironics DreamStation model. The foam was found to degrade and release harmful particles and gases Current customer recall programs Philips Respironics Sleep and Respiratory Care devices Philips Avent Video Baby Monitor Replacement Energy saver dimmable I have been involved with the recall since the beginning of recall. Latest update: On 8/2/2022, Philips has been asked by the FDA (Federal drug administration) to set your replacement CPAP for your recalled device with your pressure settings BEFORE shipping to you directly. The consent decree was the result of a series of events starting with the voluntary recall notification issued by Philips on June 14, 2021, after safety concerns were raised for certain ventilators, CPAP devices, and bilevel positive airway pressure devices because of potential health risks related to the polyester-based polyurethane sound abatement foam used in these devices. Updating contact information (including address), or to cancel a registration. But the process is taking years, forcing some patients to risk their health. Philips recall toll-free number: 877-907-7508. Sep 28, 2023 · We found answers to some of the most critical questions about the ongoing recall of millions of CPAP machines, ventilators and other breathing devices. Here’s How We Did It. Apr 10, 2024 · AASM guidance in response to Philips recall of PAP devices On June 14, 2021, Philips initiated a voluntary recall notification in the U. 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. Aug 8, 2024 · Philips Recall: What Happened? On June 14, 2021, Philips announced that it would be recalling three to four million continuous positive airway pressure (CPAP), bi-level positive airway pressure (BiPAP) and mechanical ventilator devices over risks associated with the products’ sound abatement foam. Dec 18, 2023 · Philips offers a $479M class action CPAP lawsuit settlement for eligible users of recalled sleep apnea devices. The affected products are identified in the tables below: Dec 14, 2022 · Voluntary Recall Information Philips Respironics Sleep and Respiratory Care devices News and Updates > Understand the steps we take to ensure the safety of your replacement CPAP or BiPAP device Aug 17, 2025 · The Philips CPAP recall lawyers at Miller & Zois are reviewing sleep apnea machine cases from users of the Philips CPAP or BiPAP sleep apnea machines in all 50 states. * Philips Respironics has provided the completed set of test results and analyses for the CPAP/BiPAP therapy devices to the FDA and other competent authorities. In most markets, devices currently authorized for repair and replacement include DreamStation CPAP and Bi-level devices, DreamStation ASV devices, and DreamStation ST/AVAPS devices. The sound-reducing foam inside may expose users to toxic chemicals that could cause cancer or other serious injuries. Philips kept brushing me off after repeated emails and phone calls (to the overseas call center). 1 billion settlement on April 29, 2024, to compensate people for financial damages related to the recall. Please check the US Patient Portal to take any necessary steps in receiving your replacement device as soon as possible. Jun 23, 2021 · Everything you need to know about the CPAP recall from Philips Respironics. Following the issuance of the recall notification/field safety notice* in June 2021, Philips Respironics initiated a global program to remediate the October 6, 2023 Learn more Philips response to recent media articles related to Philips Respironics’ voluntary recall notification/field safety notice September 27, 2023 Learn more July 2023 latest results and conclusions for sleep therapy devices related to the impact of ozone cleaning shows no appreciable harm to health in patients Medical Device Reports Associated with Recalled Philips Ventilators, BiPAP Machines, and CPAP Machines Jun 7, 2025 · Learn what specific BiPAP & CPAP machines made by Philips have been recalled in recent years for defects and why? We answer your questions. Together with five independent certified testing laboratories and qualified third-party experts, Philips Respironics has been conducting Jan 7, 2024 · In 2021, a widely used breathing device manufactured by Philips was the subject of a safety recall. The US Patient Portal will remain open until June 30, 2025. only). Important information for clinicians Sleep Therapy information In 2021, Philips Respironics determined from user reports and initial testing that there were possible risks to users related to the polyester-based polyurethane (PE-PUR) sound abatement foam used in specific CPAP, BiPAP and ventilator devices. Latest updates Explained: The voluntary Philips Respironics sleep and respiratory care devices recall* Latest updates Explained: The voluntary Philips Respironics sleep and respiratory care devices recall* Jul 30, 2021 · Philips Respironics (Philips) has recalled several models of its Continuous Positive Airway Pressure (CPAP) machines, BiLevel Positive Airway Pressure (BiLevel PAP) machines and mechanical ventilators in Canada and internationally. Following the issuance of the recall notification/field safety notice* in June 2021, Philips Respironics initiated a global program to remediate the On May 9, 2024, the Philips Defendants and Plaintiffs’ Negotiating Counsel (“Parties”) entered into a Master Settlement Agreement (“MSA”) to resolve actual asserted claims or potential Personal Injury Claims against the Philips Defendants concerning certain recalled CPAP, BIPAP and ventilator products (“Recalled Devices”). In addition to the number of replacement devices delivered, we also provide an overview of the number of devices that will be financially compensated and the number of devices that can no longer be traced by home care providers. Sep 21, 2024 · Users of recalled CPAP machines are receiving their share of settlements in class-action lawsuits. As we discuss below, May 16, 2023 · Testing results for affected devices In June 2021, after discovering potential health risks related to the polyester-based polyurethane (PE-PUR) sound abatement foam in certain CPAP, BiPAP and Mechanical Ventilator devices, Philips Respironics issued a voluntary recall notification. Throughout this process, I remained diligent about the following points: Verifying recall eligibility by checking official device lists. Here’s what to know about the recalled lots. In June 2021, after discovering a potential health risk related to the foam in certain CPAP, BiPAP and Mechanical Ventilator devices, Philips Respironics issued a voluntary recall notification (US only) / Field Safety Notice (outside US). Aug 24, 2025 · Our law firm was handling Philips CPAP machine lawsuits for injuries from the recalled Philips CPAP machine. Nov 29, 2023 · We understand how important Philips Respironics sleep and respiratory care devices are to patients who use them. Dec 31, 2024 · Philips Respironics will no longer accept new registrations for affected CPAP and BiPAP devices in the US after December 31, 2024. S. Sep 11, 2023 · Read the Philips CPAP machine lawsuit update 2023 to discover which sleep apnea devices were recalled and the final cost of the settlement. EST, December 31, 2024. In 2021, Philips Respironics determined from user reports and initial testing that there were possible risks to users related to the polyester-based polyurethane (PE-PUR) sound abatement foam used in specific CPAP, BiPAP and ventilator devices. Recall of CPAP, BiPAP and Ventilators relating to the PE-PUR sound abatement foam I need to update my registration information. For patients using life-sustaining mechanical ventilator devices: DO NOT discontinue or alter Dec 13, 2022 · Information around the Philips Respironics voluntary recall for certain CPAP, Bi-PAP and Ventilator Devices due to polyurethane foam used in these devices. An international team of reporters reviewed thousands of records and interviewed insiders to expose what Nov 14, 2022 · Voluntary Recall Information Philips Respironics Sleep and Respiratory Care devices News and Updates > How to return your affected device Nov 22, 2024 · Health Care How Lincare Cashed In on the Disastrous Recall of Philips Breathing Machines — at the Expense of Patients Amid reports of thousands of injuries and hundreds of deaths, Lincare was Nov 16, 2025 · Understanding the Philips CPAP Lawsuit The Philips CPAP lawsuit began after millions of CPAP, BiPAP, and ventilator devices were recalled due to the breakdown of the polyester-based polyurethane (PE-PUR) foam inside the machines. With the remediation of the sleep therapy devices almost complete and remediation of the ventilators ongoing, it is important that patients, Durable Medical Equipment providers (DMEs) and clinicians are informed on the latest updates. After careful analysis, Philips Respironics issued a Voluntary Recall Notification in the US and a Field Safety Notice in other markets. The recall notification (U. Tragically, more than 560 deaths have been linked to the devices in less than three years since the recall. Apr 7, 2023 · The 2021 recall was for 20 different Philips devices, including its A-Series BiPAP ventilators and the DreamStation CPAP machines. Registration, replacement, and next steps. Urgent Product Defect Correction in Australia (Recall for Product Correction in New Zealand) of CPAP, BiPAP and Ventilators relating to the PE-PUR sound abatement foam Voluntary recall of CPAP and Bi-Level PAP Devices and Mechanical Ventilators (sound abatement foam) Initiated June 2021 The foam that is used in some devices to reduce sound and vibration showed signs of degradation (damage) and chemical emissions. Dec 10, 2024 · Americans relying on Philips CPAP and BiPAP machines should know the potential risks and recognize the signs of exposure to the degraded foam has become paramount. Dec 11, 2021 · Today, the FDA is providing an update related to the June 14, 2021, recall of certain Philips Respironics ventilators, continuous positive airway pressure (CPAP) and bilevel positive airway On June 14, 2021, Philips Respironics issued a voluntary recall notification in the United States and a field safety notice internationally of the vast majority of models of continuous positive airway pressure (CPAP), bilevel PAP (BPAP), and mechanical ventilator devices produced over the last decade. Learn how to register, replace and clean your device, and check the latest updates and FAQs. Jun 7, 2025 · The Philips CPAP recall has led to widespread lawsuits as thousands of users claim they suffered serious health issues from defective sleep apnea machines. The process for preparing the corrections indicated in the recall notification (U. Jun 7, 2022 · View Philips Official Recall Notification HERE and register your device if you have not done so. Clinicians report that the Philips recall eroded patients’ trust in medicine and impaired patients’ and clinicians’ health and well-being. Sep 11, 2025 · Completing the Philips Respironics medical device recall remains our highest priority. Feb 14, 2025 · An online reviewer is warning about a CPAP machine recall. Feb 4, 2024 · The Food and Drug Administration says 561 deaths have been reported in connection to recalled Philips devices to treat obstructive sleep apnea and other breathing disorders. Those clips have reportedly interfered with medical metallic implants or objects in the body such as pacemakers, cardioverter defibrillators and neurostimulators. The devices include a foam component that reduces sounds from the device. Following the issuance of the recall notification/field safety notice* in June 2021, Philips Respironics initiated a global program to remediate the Nov 16, 2021 · Philips Respironics is voluntarily recalling the below devices due to two (2) issues related to the polyester-based polyurethane (PE-PUR) sound abatement foam used in Philips Continuous and Non-Continuous Ventilators: 1) PE-PUR foam may degrade into particles which may enter the device’s air pathway and be ingested or inhaled by the user, and 2) the PE-PUR foam may off-gas certain chemicals Philips CPAP and BiLevel PAP Recall Philips Respironics announced a voluntary recall for certain CPAP, BiLevel PAP, and mechanical Ventilator Devices due to issues related to deterioration of the sound abatement foam used in these devices. Medical Device Recall Information Philips Respironics Sleep and Respiratory Care devices Support, at every step of the way Understand how we’re handling the recall and know what to expect We understand that waiting for news about when and how your device will be repaired or replaced can be frustrating. Oct 25, 2022 · Philips is trying to fix or replace 5 million of the devices because foam in them can deteriorate into harmful particles. The FDA provides updates, recommendations, and resources for patients and health care providers affected by the recall. These devices, commonly used to treat sleep apnea, were recalled due to potential health risks posed by the sound abatement foam used in the machines. Voluntary Field Safety Notice Information Philips Respironics Sleep and Respiratory Care devices In June 2021, after discovering a potential health risk related to the foam in certain CPAP, BiPAP and Mechanical Ventilator devices, Philips Respironics issued a voluntary Field Safety Notice (outside U. We are focused on delivering the best care Jun 29, 2023 · Voluntary Recall Information Philips Respironics Sleep and Respiratory Care devices News and Updates > Waiting for your replacement device? Here are the actions you may need to take to continue your remediation pathway. Sep 27, 2023 · Philips Respironics provides update on filed MDRs in connection with the voluntary recall notification/field safety notice* for specific CPAP, BiPAP and mechanical ventilator devices Nov 15, 2024 · A federal judge has determined that a $25 million Philips CPAP medical monitoring settlement is “fair, reasonable and adequate”, providing funding to monitor individuals exposed to toxic foam On June 14, 2021, Philips Respironics announced a voluntary recall of all CPAP, BiPAP, and Ventilator devices manufactured prior to April 21, 2021. This toxic sound-abatement foam could degrade over time, releasing harmful particles and chemical gases into the user’s airway. Oct 4, 2022 · * This is a recall notification for the US only, and a field safety notice for the rest of the world. A CPAP class You may have heard about the 2021 voluntary Philips Respironics recall notification* related to certain CPAP and BiPAP sleep therapy devices and ventilators, and you may have questions about related litigation . 5 million recalled CPAPs and other devices — and reports of The issue relates to certain ventilators, Philips CPAP (Continuous Positive Airway Pressure) and BiPap (Bi-Level Positive Airway Pressure) sleep apnea devices. Patient safety and quality remains our top priority, and we continue to dedicate all necessary resources to ensure that impacted patients receive Jun 28, 2022 · Voluntary Field Safety Notice Information Philips Respironics Sleep and Respiratory Care devices In June 2021, after discovering a potential health risk related to the foam in certain CPAP, BiPAP and Mechanical Ventilator devices, Philips Respironics issued a voluntary Field Safety Notice (outside U. Apr 29, 2024 · Millions of CPAP sleep apnea machines made by the medical device maker Philips and a subsidiary were found to have a dangerous problem, triggering consumer lawsuits and a massive recall in 2021. We explain reasons for recalls, how to find out whether your CPAP machine is recalled, and what to do next. Philips recalled certain CPAP machines in June 2021 due to potential health risks from PE-PUR foam breakdown. Following the issuance of the recall notification/field safety notice* in June 2021, Philips Respironics initiated a global program to remediate the Voluntary Recall Information Philips Respironics Sleep and Respiratory Care devices The US Patient Portal will no longer be available after December 31, 2025. Some reworked DreamStation CPAP and BiPAP machines may have incorrect or duplicate serial numbers and deliver inaccurate or insufficient therapy. Philips Respironics issued a voluntary recall notification for certain sleep and respiratory care devices due to a potential health risk from the foam. Provides information and assistance for individuals impacted by the Philips Respironics CPAP device recall. Philips recall reimbursement timeline philips cpap recall refund Other posts Philips CPAP Recall Support Group Brenda HaleySep 10 Voluntary Recall Information Philips Respironics Sleep and Respiratory Care devices The US Patient Portal will no longer be available after December 31, 2025. Subsequently Dec 21, 2022 · We know that patients depend on Philips Respironics devices for their health and well-being. This private Settlement Program is intended to resolve Philips Respironics is voluntarily recalling the below devices due to two (2) issues related to the polyester-based polyurethane (PE-PUR) sound abatement foam used in Philips Continuous and Non-Continuous Ventilators: 1) PE-PUR foam may degrade into particles which may enter the device’s air pathway and be ingested or inhaled by the user, and 2) the PE-PUR foam may off-gas certain chemicals Oct 23, 2023 · In 2021, Philips Respironics determined from user reports and initial testing that there were possible risks to users related to the polyester-based polyurethane (PE-PUR) sound abatement foam used in specific CPAP, BiPAP and ventilator devices. See if you may be able to file a Philips CPAP lawsuit to pursue compensation and justice. Many individuals reported developing The federal court entered a consent decree against Philips Respironics following a recall of certain sleep therapy machines manufactured by the company. Philips Respironics is voluntarily recalling the below devices due to two (2) issues related to the polyester-based polyurethane (PE-PUR) sound abatement foam used in Philips Continuous and Non-Continuous Ventilators: 1) PE-PUR foam may degrade into particles which may enter the device’s air pathway and be ingested or inhaled by the user, and 2) the PE-PUR foam may off-gas certain chemicals Aug 27, 2021 · Philips will provide further clarity on projected dates for implementation of the correction to begin when this information is available. only) / field safety notice (International Markets) has begun. On May 9, 2024, the Philips Defendants and Plaintiffs’ Negotiating Counsel (“Parties”) entered into a Master Settlement Agreement (“MSA”) to resolve actual asserted claims or potential Personal Injury Claims against the Philips Defendants concerning certain recalled CPAP, BIPAP and ventilator products (“Recalled Devices”). only) / field safety notice (International Markets) advises patients and customers to take the following actions: For patients using BiLevel PAP and CPAP devices: Discontinue use of affected units and consult with physicians to determine the benefits of continuing therapy and potential risks. Nov 7, 2025 · The Philips CPAP lawsuit started with a major recall initiated by Philips, a leading electronics company, regarding their Continuous Positive Airway Pressure (CPAP) machines. Dreamstation 2 is not affected. 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 (International markets) / voluntary recall notification (U. [Image courtesy of Philips] There are 5. recall (and an international field safety notice) for specific Philips Respironics models of continuous positive airway pressure (CPAP), bilevel positive airway pressure (BPAP), and mechanical ventilator devices. Urgent Product Defect Correction in Australia (Recall for Product Correction in New Zealand) of CPAP, BiPAP and Ventilators relating to the PE-PUR sound abatement foam Nov 16, 2021 · Philips Respironics CPAP and Bi-Level PAP Devices Sound Abatement Foam Susceptibility to Degradation and Volatile Organic Compound Emission Aug 5, 2024 · But in 2021, Philips issued a global recall of Lynch’s CPAP machine and several other models – 15 million in total, all sold between 2008 and 2021. Sleep and respiratory care updatesThe notification advises patients and customers to take the following actions: For patients using BiLevel PAP and CPAP devices: Discontinue use of affected units and consult with physicians to determine the benefits of continuing therapy and potential risks. We deeply regret that for many patients, the voluntary recall notification to address potential health risks related to the polyester-based polyurethane (PE-PUR) sound abatement foam in specific CPAP, BiPAP and mechanical ventilator devices has created uncertainty and concern. CPAP and BiPAP machines are medical devices used for the treatment of obstructive sleep apnea. According to the recall notice, the polyester-based polyurethane (PE-PUR) foam may break down UPDATE (2024-07-05): Update on Philips Respironics recall of several models of CPAP and BiLevel PAP machines and mechanical ventilators Since 2021, Philips Respironics (Philips) has established a registration portal, as a part of their repair and replacement program, for affected CPAP and BiLevel PAP machines and mechanical ventilators in Canada. Feb 8, 2022 · Voluntary Recall Information Philips Respironics Sleep and Respiratory Care devices News and Updates > Ozone Cleaner Information Recalled Philips Ventilators, BiPAP Machines, and CPAP Machines News Release: FDA Provides Update on Recall of Certain Philips Respironics Breathing Assistance Machines (November 12, 2021) Dec 29, 2024 · Advertisement Investigation update: After massive CPAP recall, Philips plagued by more fallout Pittsburgh medical device giant moves manufacturing to Thailand in wake of more recalls Below is an update on the status of our repair and replacement program for impacted CPAP, BiPAP and mechanical ventilator devices as of October 31, 2024. The FDA is still considering the data and analyses that Philips Respironics has provided and may reach different conclusions. This recall affects CPAP and BiLevel PAP devices manufactured prior to April 26, 2021. Jan 29, 2024 · Philips announced a recall for millions of their Bi-Level Positive Airway Pressure (Bi-Level PAP), Continuous Positive Airway Pressure (CPAP), and mechanical ventilator devices in 2021. May 10, 2024 · In June 2021, Philips recalled several CPAP, BiPAP and ventilator machines because sound abatement foam could degrade and cause serious health problems. The affected products are identified in the tables below: The issue relates to certain ventilators, Philips CPAP (Continuous Positive Airway Pressure) and BiPap (Bi-Level Positive Airway Pressure) sleep apnea devices. m. May 28, 2024 · Philips Respironics has issued a medical device recall regarding interruptions and/or loss of therapy in the Philips Respironics OmniLab Advanced Plus (OLA+), V30 Auto, BiPAP A30, and BiPAP A40. Sep 27, 2023 · Health Care We Spent a Year Investigating the Philips CPAP Recall. Philips Respironics CPAP and BiPAP machines contain a type of foam – polyester-based polyurethane – that can break down, releasing chemicals that can be Oct 31, 2023 · Tracking Philips Respironics recalls Philips has issued numerous recalls of its sleep apnea devices and ventilators, affecting millions of devices, since first disclosing problems with soundproofing foam used in the machines in 2021. In June 2021, Philips initiated a voluntary recall notification* for certain continuous positive airway pressure (CPAP) and bi-level positive airway pressure (BiPAP) sleep therapy devices and ventilators related to the polyester-based polyurethane (PE-PUR) sound abatement foam in these devices. Oct 6, 2023 · Philips’ first priority is the health and well-being of patients, both in terms of providing replacement devices and testing to seek more clarity on the safety of the sleep and respiratory care devices under the recall. * This is a recall notification for the US only, and a field safety notice for the rest of the world. Jun 14, 2021 · Philips issues recall notification to mitigate potential health risks related to the sound abatement foam component in certain sleep and respiratory care devices. Generally prohibits Philips from exporting for commercial distribution CPAP and BiPAP devices that are being used to remediate patients impacted by the recall unless certain conditions are met, as Feb 7, 2024 · Recalled sleep apnea (CPAP and BiPAP) machines from Phillips have been tied to over 500 deaths. The devices are manufactured with a Polyester-Based Polyurethane (PE-PUR) sound abatement foam, which degrades . Learn about the Philips recalls, concerns regarding replacements, and lawsuits. Apr 11, 2024 · Several CPAP machines have been recalled. Apr 15, 2024 · Worried about the Philips CPAP recall? Learn about which devices are affected, the potential health risks, and what steps to take if you use a Philips CPAP. In the US, the recall notification has been classified by the FDA as a Class I recall. The recalled ventilator machines are normally used by people suffering from sleep apnea. This has been the main culprit behind the recall and lawsuits. Registration for affected CPAP and BiPAP devices in the US and Canada closed on December 31, 2024. Dec 14, 2022 · Voluntary Recall Information Philips Respironics Sleep and Respiratory Care devices News and Updates > The Patient Portal: Why you should use it and what to expect At the time the recall notification/field safety notice* was issued, Philips Respironics relied on an initial, limited data set and toxicological risk assessment, and assumed a worst-case scenario for the possible health risks out of an abundance of caution. Study Impact: Our results demonstrate the pervasive impact of the recall on sleep apnea care. In June 2021, Philips Respironics (Philips) recalled certain ventilators, bi-level positive airway pressure (also known as Bilevel PAP, BiPAP, or BPAP) machines, and continuous positive airway Jul 9, 2025 · Recalls of a popular brand of CPAP machine have affected millions of Americans. Now, new reporting shows that the replacement machines sent out to customers might also pose Jan 25, 2023 · RECALL NOTICE: PHILIPS RESPIRONICS CPAP AND BIPAP DEVICES Registration for affected CPAP and BiPAP devices in the US and Canada ends at 11:59 p. Information for patients May 16, 2023 · Voluntary Recall Information Philips Respironics Sleep and Respiratory Care devices In June 2021, after discovering a potential health risk related to the foam in certain CPAP, BiPAP and Mechanical Ventilator devices, Philips Respironics issued a voluntary Field Safety Notice (outside U. Philips Respironics agreed to a $1. If you or a loved one used a recalled Philips CPAP, BiPAP, or ventilator device and later developed health complications, you may be entitled to compensation. 1 billion settlement to resolve personal injury claims related to its recalled CPAP, BiPAP, and ventilator devices. With regard to mechanical ventilators, Philips is deploying a permanent corrective action to address the issues described in the recall notification. The FDA said that Nov 3, 2025 · Philips CPAP lawsuits claim people who used devices included in the 2021 CPAP recall developed cancer, lung problems or other injuries due to degraded foam. Apr 1, 2025 · In June 2021, Philips Respironics announced that certain ventilators in the company’s CPAP and BiPAP range were being recalled due to health risks. (and an international field safety notice) for specific Philips Respironics models of continuous positive airway pressure (CPAP), bilevel positive airway pressure (BPAP), and mechanical ventilator devices, stating that the recall is to “ensure patient May 16, 2023 · Full test results are also available to clinicians. 5 million sleep apnea devices. This private Settlement Program is intended to resolve Apr 15, 2024 · Worried about the Philips CPAP recall? Learn about which devices are affected, the potential health risks, and what steps to take if you use a Philips CPAP. A June 2021 recall of a number of CPAP and BiPAP devices from In June 2021, Philips Respironics issued a voluntary recall notification for specific CPAP and BiPAP devices due to an issue related to the polyester-based polyurethane (PE-PUR) foam that is used to decrease the sound within the devices.