With your MyPhilips account you can: Access all your product information in one place (orders, subscriptions, etc.) This impacts Philips Respironics CPAP and BiPAP devices sold worldwide prior to April 26, 2021. benefits outweigh the risks identified in the recall notification. To decide on the next steps, discuss the benefits and risks based on your individual health situation with your health care provider, such as your primary care physician or sleep doctor. The FDA has reached this determination based on an overall benefit-risk assessment. Very small particles from the foam could break lose and come through the air hose. Have the product at hand when registering as you will need to provide the model number. What information do I need to provide to register a product? You are about to visit a Philips global content page. Review the recommendations above with patients who use the recalled devices, including that for some patients, stopping use of the device may involve greater risk than continuing to use the recalled device. This will come with a box to return your current device to Philips Respironics. I am experiencing technical issues with the Patient Portal. The results from the independent testing are needed to determine if the silicone-based foam used in the repaired devices does in fact present any risks to patients, and the FDA will communicate those results to the public as soon as they are available. Please watch the video below from fellow Veteran and CPAP user, Dr. Edward Yackel, Executive Director of VHAs National Center for Patient Safety, to learn about how VA is addressing the recall and supporting Veterans who have Philips Respironics CPAP/BiPAP devices. Breathing in chemicals or swallowing small pieces of foam that has broken apart could potentially result in serious injury, cause permanent impairment, and require medical intervention to prevent permanent injury. Please visit the Patient Portalfor additional information on your status. The recall notification (U.S. only) / field safety notice (Outside of U.S.) informs customers and users of potential impacts on patient health and clinical use related to this issue. You can register your device at https://www.philipssrcupdate.expertinquiry.com or call their registration line at 877-907-7508. The FDA's evaluation of the information provided by Philips is ongoing. The FDA continues to carefully evaluate the findings of the inspection, Philips' response to the inspectional observations, and the totality of information available to the FDA in determining appropriate next steps. Philips Respironics Sleep and Respiratory Care devices, If you haven't yet registered your device, Important update to Philips US recall notification, Philips has updated the US recall notification to align with the, * This is a recall notification for the US only, and a field safety notice for the rest of the world. UPDATE - December 22, 2022: The FDA issued a safety communication to provide additional information to patients, caregivers, and health care providers about two recent issues in certain reworked Philips Respironics (Philips) Trilogy 100 and Trilogy 200 ventilators. The .gov means its official.Federal government websites often end in .gov or .mil. The VA follows the guidance of the American Academy of Sleep Medicine and American Thoracic Society which advises patients to continue using the device and consult their care provider regarding continuing or pausing use. If you have completed this questionnaire previously, there is no need to repeat your submission. Once your order is placed the order number will be listed in the Patient Portal. On May 2, 2022, the FDA's Center for Devices and Radiological Health (CDRH) sent notice to Philips that CDRH is proposing that an order should be issued, under section 518(b) of the Federal Food, Drug, and Cosmetic Act [a 518(b) order], to require Philips to submit a plan for the repair, replacement, or refund of the purchase price of recalled devices manufactured after November 2015. Only clean your device according to the manufacturers recommendations. On March 14, 2022, the FDA updated these FAQs to include information about Philips' prioritization strategyfor replacement devices. Click here to register a device affected by the recall of certain Philips Respironics Sleep and Respiratory Care devices Sign in now New to My Philips? In June 2021, Philips recalled certain ventilators, BiPAP machines, and CPAP machines (see table below) because of potential health risks. This recall affects CPAP and BiLevel PAP devices manufactured prior to April 26, 2021. A wide range of injuries have been reported in these MDRs, including cancer, pneumonia, asthma, other respiratory problems, infection, headache, cough, dyspnea (difficulty breathing), dizziness, nodules, and chest pain. The data collected will be used to help to prioritize remediation of those patients at higher risk. the .gov website. You can log in or create one here. If you would like to find the latest information and updates, stay connected with us or read our FAQs, please click below. Any links to third-party websites that may appear on this site are provided only for your convenience and in no way represent any affiliation or endorsement of the information provided on those linked websites. The FDA has requested that Philips retain an independent laboratory to perform additional testing to determine what, if any, potential safety risks may be posed to patients by the silicone-based foam. CDRH will consider the response when it is received. First, determine if you are using one of the affected devices. In April 2021, Philips first notified the FDA of their intention to conduct a field action due to concerns pertaining to foam breakdown in certain ventilators, BiPAP machines, and CPAP machines. More information on medical device recalls, including What is a Medical Device Recall, is available on FDA.gov. If you have any concerns we suggest you contact your durable medical equipment provider or your sleep specialist.Per Philips Respironics, all patients using one of their PAP devices should discontinue use immediately due to the health risks. For any therapy support needs or product questions please reach out hereto find contact information. Not yet registered? Continuous Positive Airway Pressure (CPAP) devices, Bi-Level Positive Airway Pressure (BiLevel PAP) devices, and, Or by calling 877-907-7508 (Spanish translation available but the patient will still need to go online to register their device). Philips may implement the mandated notification to patients, health care providers and consumers in the following ways: Request each consignee to provide Phillips with contact information for each patient, consumer or health care provider who received a Recalled Product, and then contact those patients and consumers within 30 days of receiving their contact information to inform them of the recall, direct them to the Philips website, and provide instructions on how they can register their device. Understand how were 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. CHEST MEMBERSHIP About Membership . This will allow all end users to make informed decisions regarding the risks of continued use of the Recalled Products while awaiting a replacement device. If we have attempted to reach you through multiple avenues the request may appear very generic in nature and will contain a Philips Respironics customer service number. More information on medical device recalls, including What is a Medical Device Recall, is available on FDA.gov. Please check the Patient Portal for updates. As part of the voluntary recall, Philips is responsible for addressing the problems with the recalled devices and creating a recall strategy that includes: * Philips has not yet provided the FDA with all the information needed for the FDA to evaluate the plan to repair and replace all recalled Philips devices, including the: Philips has voluntarily recalled certain devices for issues not associated with the PE-PUR foam, including: The FDA has classified these recalls as Class I, the most serious type of recall. a. Due to the volume of units affected, VHA sleep clinics may need to alter day-to-day operations as they support Veterans impacted by the recall. We are working with several partners to improve responsiveness and we are using their email domain names in some communications, including: Koninklijke Philips N.V., 2004 - 2023. There are no updates to this guidance. Follow the manufacturer's instructions and recommended cleaning and replacement guidelines for your CPAP machine and accessories. Images may vary. We are aware that Philips Respironics said to stop using your CPAP or BiPAP device. I have general DreamMapper questions or DreamMapper connection issues. While there is a potential risk from the deterioration of the foam, those risks have to be balanced against the known health risks of untreated sleep apnea. Our site can best be viewed with the latest version of Microsoft Edge, Google Chrome or Firefox. You can also upload your proof of purchase should you need it for any future service or repairs needs. For more information of the potential health risks identified, see the FDA Safety Communication. Those being treated for sleep apnea by the WTC Health Program may be using one of the impacted machines. Questions regarding registration, updating contact information (including address), or to cancel a registration. To register a new purchase, please have the product on hand and log into your My Philips account. See the FDA Safety Communication for more information. . Registration Link: https://www.usa.philips.com/healthcare/e/sleep/communications/src-updateWe wanted to share our step-by-step walkthrough of the process to . Your replacement device will include three key pieces of information, including how-to: If you need more information, scan the QR codes and call our support team at +1-833-262-1871 with any questions. No. Office of Accountability & Whistleblower Protection, Training - Exposure - Experience (TEE) Tournament, Chief Resident in Quality and Patient Safety, About the National Center for Patient Safety, War Related Illness & Injury Study Center, Clinical Trainees (Academic Affiliations), https://www.philipssrcupdate.expertinquiry.com, Call TTY if you If youre interested in providing additional information for the patient prioritization, check your order status. More information on. The FDAs in-depth review and analysis of these new MDRs will include examining the possible reasons for the increased number of reports. Patients who have additional concerns should talk to their health care provider about the plan for their care and treatment. More information is available at http://www.philips.com/src-update. How can I register my product for an extended warranty? You may have to contact your care provider to program the device to your prescribed settings. This guidance has been updated from our previous recommendation to stop therapy before consulting withyour physician. As the situation is constantly evolving, we will continue to make sure that both you and your care team have the most up-to-date information until you receive your replacement device. In this video, we will be going into detail about the process to register your device on the Philips website. Following two rounds of comprehensive customer and patient outreach, Philips Respironics has reached the vast majority of the installed base in the US resulting in the registration of approximately 2.6 million devices in the country. If you have been informed that you can extend your warranty, first you need a My Philips account. Clinical information has been made available to your care teams to help them make the best decision aboutyour treatment plan. The U.S. Food and Drug Administration (FDA) is updating the June 2021 safety communication about the Philips Respironics (Philips) recalled ventilators, bilevel positive airway pressure (also. For further information about your current status, please log in to the. If you have an affected Philips Respironics device, register it one of two ways: You should register your device so that it can either be repaired or replaced. The FDA continues to review and assess MDRs and will keep the public informed as new information becomes available. 2. The FDA is committed to assuring that Philips takes appropriate steps to correct the devices, working with other manufacturers and government partners to try to help make available more CPAP and BiPAP machines, and addressing concerns and questions raised by patients and health care providers about device replacement. VA clinical experts are working with the FDA and the manufacturer to understand those risks. The silicone foam material used to replace the PE-PUR foam in the reworked ventilators may potentially move and block the airpath, which may reduce air flow in the ventilator and could also cause the device to alarm. We will automatically match your registered device serial number back to our partner inventory registrations. Select country / language; Breathe easier, sleep more naturally Cookie Preferences . Before sharing sensitive information, make sure you're on a federal government site. Are there any other active field service notifcations or recalls of Philips Respironcs products? Phillips Respironics has identified a problem with a breakdown of the foam material used for sound reduction in their CPAP and BiPAP devices. classified by the FDA as a Class I recall. You are about to visit a Philips global content page. kidneys and liver) and carcinogenic effects. Create account Create an account Already have an account? Then you can register your product. We may request contact information, date of birth, device prescription or physician information. b. The more we know about these devices the more research we can do.". At this time no serious adverse health events have been reported but Philips Respironics has received reports of headache, upper airway irritation, cough, chest pressure and sinus infection. Read more in the safety communication for Certain Reworked Philips Respironics Trilogy 100/200 Ventilators Recalled Due to Potential for Silicone Foam Adhesion Failure and Residual PEPUR Foam Debris. Apologize for any inconvenience. Devices authorized for repair and replacement include DreamStation CPAP and BiLevel devices, DreamStation ASV devices, and DreamStation ST/AVAPS devices. You must register your recalled device to get a new replacement device. Philips has pre-paid all shipping charges. Philips Respironics states that the likelihood of foam breakdown is higher in devices that are more than three years old, are used in high heat (more than 95 degrees) and high humidity environments or that were routinely cleaned with an ozone cleaning device. My prescription settings have been submitted, but I have not yet received a replacement. Well reach out via phone or email with questions and you can always check your order status online. Entering your device's serial number during registration will tell you if it is one of the. We are currently reaching out to some patients via email, mail and phone and will ask for additional information to complete certain remediations. We understand that waiting for news about when and how your device will be repaired or replaced can befrustrating and that timing is critical. Our focus, as always, remains committed to remediating devices, and at this time we are starting order fulfillment for those that are already matched. Philips Respironics Sleep and Respiratory Care devices, 2. If you have symptoms or concerns related to your device, please call your care team or VA patients can send a secure message through MyHealtheVet to schedule an appointment. Philips makes no representations or warranties of any kind with regard to any third-party websites or the information contained therein. You can still register your device on DreamMapper to view your therapy data. Ozone cleaners may worsen the breakdown of the foam, even if you do not see pieces of the foam in the air tubes. Since your physician knows your medical history, they are the most qualified person todetermine the benefit or risk of staying on your therapy until you receive your replacement device. The website provides you current information on the status of the recall and how to receive permanent corrective action to address the two (2) issues. Call us at +1-877-907-7508 to add your email. You will now be able to tab or arrow up or down through the submenu options to access/activate the submenu links. In the US, the recall notification has been. These Philips Trilogy 100 and Trilogy 2000 ventilators were a part of this recall in June 2021 for issues with the polyester-based polyurethane (PE-PUR) sound abatement foam breakdown. See Potential Risks Associated With The Use of Ozone and Ultraviolet (UV) Light Products for Cleaning CPAP Machines and Accessories. Similar testing provided by Philips to the FDA on devices authorized for marketing in the U.S. had demonstrated acceptable results. Work with consumers, patient organizations, and health care professional societies to understand and address common questions and concerns related to this recall. Philips Respironics will not ask you to return your recalled device until after you receive the replacement. Access all your product information in one place (orders, subscriptions, etc. Your provider may advise you to: Stop using your recalled device (see How to Know if You Should Stop Using Your Device in. Maintain prominently displayed information on the risk of using ozone cleaners on the Recalled Products on the Philips Recall main landing page. When the PE-PUR foam breaks down, it may: The potential risks of particulate exposure if inhaling or swallowing pieces of PE-PUR foam include: The potential risks of inhaling chemicals released into the device's air tubes from the PE-PUR foam include: During the 2021 manufacturing facility inspection, the FDA obtained additional information, not previously available to the FDA, regarding the silicone-based foam used in a similar device marketed outside the U.S., which failed one safety test for the release of VOCs. If you have a health issue, including any of the health issues listed above, or any problem with your device, the FDA encourages you to talk to your health care provider and report the problem through the MedWatch Voluntary Reporting Form. You can log in or create one. Due to technical reasons, we are currently not supporting registrations for medical devices like CPAP and BIPAP. Currently, while this independent testing is performed, the FDA does not recommend that patients who have participated in the repair and replace program discontinue use of their product. Membership. Please note: only certain devices made by Philips are subject to this recall. We recognize that patients rely on these devices, and we are closely monitoring the company's actions to ensure that the issues are resolved in a timely manner given the impact on patients. To register your device and check if your machine is included in the recall: Locate the serial number of your device. Dont have one? Philips CPAP Recall Information. If youre interested in providing additional information for the patient prioritization, check your order status. The devices are used to help breathing. The FDA recognizes that many patients have questions about what this information means for the status of their devices. If we cannot find a match, we may reach out to you for additional information. News and Updates> Important update to Philips US recall notification. Do not stop or change ventilator use until you have talked to your health care provider. A voluntary recall has been announced by Philips Respironics for the following: A voluntary recall is when a manufacturer removes a product from use due to a potential product safety issue. SignUp or Login here For any therapy support needs or product questions please reach out hereto find contact information. All rights reserved. On June 14, 2021, Philips Respironics issued a voluntary recall of its CPAP, BiPAP and mechanical ventilator devices. There are no updates to this guidance. For further information about your current status, please log in to the Patient Portal or call 877-907-7508. Is there a question we can answer for you? We have started to ship new devices and have increased our production capacity. Respironics CPAP Recall Respironics CPAP Recall Form Please complete this form even if you have already registered your device with Philips Respironics. The FDA recommended, and Philips has agreed, to implement a prioritization approach that ensures patients who are most vulnerable to poor health care outcomes with continued use or ceasing use of the Recalled Products receive replacement devices as quickly as possible. Creating a plan to repair or replace recalled devices. Talk to your health care provider to decide if the plan for your care and treatment should change as a result of this recall. hb```:mAd`0pl`:aZ A0v0D4H4v%e9b> c, SC2S%MX h?>~LJ3AF E : Philips Respironics created an online registration process to allow patients to look up their device serial number . The company formally submitted their Report of Correction and Removal (a report under 21 CFR part 806, or 806 report) in June 2021. Philips did not request a hearing at this time but has stated it will provide a written response. Due to technical reasons, we are currently not supporting registrations for medical devices like CPAP and BIPAP. Why do I need to upload a proof of purchase? While we havealready made progress in shipping replacement devices, and have increased our production capacity, weanticipate the repair and replacement program in the US will take through approximately September 2022to complete. Philips Respironics issued a statement on September 1, 2021 informing United States-based customers of its new repair and replacement program for first-generation DreamStation devices in relation to the June 14, 2021 recall notification.The vast majority of the registered affected devicesmore than 80%are from the first-generation DreamStation product family, and more than half of the . Selected products An official website of the United States government, Recalls, Market Withdrawals and Safety Alerts, FAQs on Philips Respironics Ventilator, BiPAP Machine, and CPAP Machine Recalls, Certain Reworked Philips Respironics Trilogy 100/200 Ventilators Recalled Due to Potential for Silicone Foam Adhesion Failure and Residual PEPUR Foam Debris, How to Tell if Your Device Has Been Recalled and What to Do Next, How to Know if You Should Stop Using Your Device, What to Do with Your Device: Cleaners, Filters, Foam, Returns, Philips' Recalls Not Associated with the Foam Issue, How to Report a Health Issue or Problem to the FDA, FDA Safety Communication: Update: Certain Philips Respironics Ventilators, BiPAP, and CPAP Machines Recalled Due to Potential Health Risks: FDA Safety Communication, How to Locate the Serial Number on your device, report the problem through the FDA's MedWatch Voluntary Reporting Form, Potential Risks Associated With The Use of Ozone and Ultraviolet (UV) Light Products for Cleaning CPAP Machines and Accessories, recall of certain Trilogy EVO Ventilators for potential health risks from PE-PUR foam, requested that Philips retain an independent laboratory to perform additional testing of the silicone-based foam, Philips Respironics Recalls Certain Masks for BiPAP, CPAP Machines Due to Safety Issue with Magnets That May Affect Certain Medical Devices, Philips Respironics Recalls Certain BiPAP Machines for Plastic Issue that May Expose Patients to Certain Chemicals of Concern, Philips Respironics Recalls All V60 and V60 Plus Ventilators for Power Issue that May Cause Ventilator to Stop with or without Alarms, Philips Respironics Recalls V60 and V60 Plus Ventilators for Expired Adhesive that May Cause Ventilator to Stop Working With or Without an Alarm, Philips Respironics Recalls V60 and V60 Plus Ventilators Equipped with High Flow Therapy Software Versions 3.00 and 3.10 Due to Risk of Receiving Reduced Oxygen, report the problem through the MedWatch Voluntary Reporting Form, Philips' medical device recall information page. 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