respironics recall registration
You will now be able to tab or arrow up or down through the submenu options to access/activate the submenu links. Irritation to the skin, eyes, nose, and respiratory tract (airway), Toxic or cancer-causing effects to organs, such as kidneys and liver, Irritation in the eyes, nose, respiratory tract (airway), and skin, Hypersensitivity reaction, such as an allergic reaction or another immune system reaction. We are aware that Philips Respironics said to stop using your CPAP or BiPAP device. For further information about your current status, please log into the portal or call 877-907-7508. 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. We will never request the following information from you over phone or email: social security number, bank or financial information, insurance information. Page Last Reviewed: August 2, 2021 | Page Last Updated: August 2, 2021. The FDAs in-depth review and analysis of these new MDRs will include examining the possible reasons for the increased number of reports. Didn't include your email during registration? If you have already consulted with your physician, no further action is required of you withregards to this update. endstream endobj 273 0 obj <>/Metadata 11 0 R/Pages 270 0 R/StructTreeRoot 18 0 R/Type/Catalog/ViewerPreferences 288 0 R>> endobj 274 0 obj <>/MediaBox[0 0 612 792]/Parent 270 0 R/Resources<>/Font<>/ProcSet[/PDF/Text/ImageB/ImageC/ImageI]>>/Rotate 0/StructParents 0/Tabs/S/Type/Page>> endobj 275 0 obj <>stream Well reach out via phone or email with questions and you can always check your order status online. All rights reserved. I was instructed to upload my prescription settings to Philips Respironics through DreamMapper and am experiencing issues. Philips submitted 30 MDRs between 2011-April 2021 that they identified as associated with the PE-PUR foam degradation (breakdown). The FDA is aware that patients have already received devices with silicone-based foam as part of the repair and replace program. Contact and support for Philips Respironics voluntary recall Voluntary Recall Information Philips Respironics Sleep and Respiratory Care devices I would like to speak with someone. Follow Philips' instructions for recommended cleaning of your CPAP machine and accessories. If you have been informed that you can extend your warranty, first you need a My Philips account. For a list of the affected devices and more information regarding the recall from Philips Respironics you can go to: https://www.usa.philips.com/healthcare/e/sleep/communications/src-updateChapters:00:00 Intro00:44 Find Your Serial Number01:49 Online Form06:05 Demand for CPAP MachinesShop Online: Our Store: https://sleeplay.comCPAP Machines: https://sleeplay.com/collections/cpap-machinesCPAP Masks: https://sleeplay.com/collections/cpap-masksCPAP Cleaning: https://sleeplay.com/collections/cpap-cleaningCPAP Supplies: https://sleeplay.com/collections/cpap-suppliesOxygen Therapy: https://sleeplay.com/collections/oxygen-therapyGo Social:Facebook: https://facebook.com/sleeplaygroundInstagram: https://instagram.com/sleeplaygroundTwitter: https://twitter.com/sleeplayground TikTok: https://tiktok.com/@sleeplaygroundBecome an Affiliate:https://sleeplay.refersion.com/affiliate/registrationFree Consultation:https://calendly.com/sleeplay/respiratory-therapist-consultation In the US, the recall notification has been classified by the FDA as a Class I recall. This recall affects CPAP and BiLevel PAP devices manufactured prior to April 26, 2021. Secure .gov websites use HTTPS We have started to ship new devices and have increased our production capacity. Your provider may advise you to: Stop using your recalled device (see How to Know if You Should Stop Using Your Device in. If you would like to find the latest information and updates, stay connected with us or read our FAQs, please click below. 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. I would like to learn more about my replacement device. Only clean your device according to the manufacturers recommendations. On March 10, 2022, the FDA issued a notification order under section 518(a) of the Federal Food, Drug, and Cosmetic Act [a 518(a) order] to Philips requiring the company to notify patients and others of the company's June 14, 2021, recall and the unreasonable risk of substantial harm to the public health posed by the degradation of the PE-PUR sound abatement foam used in the recalled products because the company's notification efforts to date have been inadequate. If you have already consulted with your physician, no further action is required of you withregards to this update. The devices included are CPAP machines due to issues related to the polyester-based polyurethane sound abatement foam used in its continuous and non-continuous ventilators. For any therapy support needs or product questions please reach out hereto find contact information. The polyester-based polyurethane (PE-PUR) foam used in these medical devices to lessen sound and vibration can break down. You will need to keep and clean these to use with your replacement device, Using packing tape supplied, close your box, and seal it, Affix the pre-paid postage label to the box and schedule a pick up at your local FedEx. During the manufacturing facility inspection, the FDA obtained information, not previously available to the agency, regarding the silicone-based foam used in a similar device marketed outside the U.S., which failed one safety test for the release of certain chemicals of concern, called volatile organic compounds (VOCs). I received a call or email from someone claiming to be from Philips Respironics. classified by the FDA as a Class I recall. The FDA is ordering Philips Respironics to notify all device users, durable medical equipment (DME) suppliers, distributors, retailers, and health care providers who prescribe the products about. Three types of devices have been recalled: 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 Trilogy 100 and Trilogy 200 ventilators. To access the menus on this page please perform the following steps. 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. What information do I need to provide to register a product? The site is secure. Call us at +1-877-907-7508 to add your email. If you do not find your device on the list of recalled models or during registration: You may want to contact the medical equipment supplier (commonly known as a Durable Medical Equipment (DME) supplier) who gave you your device. At this time, the FDA is not changing the recommendations from the previous June 2021 safety communication. Be cautious as they may be scams! No. On February 9, 2023, the FDA provided an update on the medical device reports (MDRs) received by the FDA. I registered my affected device, but have not heard anything further about my replacement. Carefully evaluate the totality of information available to the FDA in determining appropriate next steps. The FDA classified the recall of certain Trilogy Evo ventilators as a Class I recall, the most serious type of recall. Philips Respironics is the leading provider of innovative solutions for the global sleep and respiratory markets. Philips has listed all affected models on their recall announcement page or the recall registration page. Follow the recommendations above for the recalled devices used in health care settings. The foam was determined to be PE-PUR foam, the same type of foam used in Philips' devices previously recalled in June 2021. While we work to provide patients with a replacement device as quickly as possible, we want you to feel informed about each step of the remediation process, and confident in your new device. We recommend you upload your proof of purchase, so you always have it in case you need it. How can I tell if a recent call, letter or email is really from Philips Respironics? Cleaning, setup and return instructions can be found here. In December 2021, Philips initiated the recall of certain Trilogy EVO Ventilators for potential health risks from PE-PUR foam. %PDF-1.7 % Our physicians have had many meetings with the manufacturer as well as with other sleep medicine practices, and we currently recommend the following: Call Philips Respironics at 1-877-907-7508 to register your device or register your device via the web at: https://www.philipssrcupdate.expertinquiry.com/ 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. A locked padlock The website also provides you instructions on how to locate your device Serial Number and will guide you through the registration process. 2. Philips Sleep and respiratory care. For more information on the company's recall notification, contact your local Philips representative or visit Philips' medical device recall information page. Use another similar device that is not a part of this recall. The company formally submitted their Report of Correction and Removal (a report under 21 CFR part 806, or 806 report) in June 2021. . Selected products Lock On June 14, 2021, Philips Respironics sent customers an "Urgent: Medical Device Recall" letter requesting them to take the following actions: Discontinue use of the device and work with a. We are currently reaching out to some patients via email, mail and phone and will ask for additional information to complete certain remediations. By clicking on the link, you will be leaving the official Royal Philips Healthcare ("Philips") website. Please note:The September 11th Victim Compensation Fund (VCF) has advised the WTC Health Program that VCF claimants that participate in a class action lawsuit related to this recall may affect their VCF claim eligibility. Home | Philips Recall (expertinquiry.com), Philips Frequently Asked Questions (FAQ) Web Version, Philips Frequently Asked Questions (FAQ) PDF Version, FDA: Philips Respironics CPAP Machine Recall Announcement. Work with other manufacturers and government partners to try to help make available more BiPAP and CPAP machines. See Potential Risks Associated With The Use of Ozone and Ultraviolet (UV) Light Products for Cleaning CPAP Machines and Accessories. Ozone cleaners may worsen the breakdown of the foam, even if you do not see pieces of the foam in the air tubes. Throughout the remediation process, we are working closely with our partners to determine the best way to repair or replace an affected 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. For your immediate reference, the July 9, 2021 joint position statement by The Canadian Thoracic Society, Canadian Sleep Society and the Canadian Society of Respiratory Therapists states: . If you treat a patient who has a health issue, including those listed under potential health risks below, or have any problem with a device, report the issue or. We recommend you upload your proof of purchase, so you always have it in case you need it. My issue is not addressed here. We are currently reaching out to some patients via email, mail and phone and will ask for additional information to complete certain remediations. Maintain prominently displayed information on the risk of using ozone cleaners on the Recalled Products on the Philips Recall main landing page. The .gov means its official.Federal government websites often end in .gov or .mil. The FDA's evaluation of the information provided by Philips is ongoing. You are about to visit the Philips USA website. Inline bacterial filters may increase the resistance to air flow through the device, which could mean the ventilator will not ventilate adequately. b. See the FDA Safety Communication for more information. Have the product at hand when registering as you will need to provide the model number. Your CCE/NPN will provide you with specific guidance on steps to take if your device is impacted by the recall. 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. The devices are used to help breathing. 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. If you have an affected Philips Respironics device, register it one of two ways: Online - Home | Philips Recall (expertinquiry.com) Or by calling 877-907-7508 (Spanish translation available but the patient will still need to go online to . I have general DreamMapper questions or DreamMapper connection issues. Dont have one? To register a new purchase, please have the product on hand and log into your My Philips account. To register your product, youll need to log in to your My Philips account. All rights reserved. Philips Respironics recalled several models of DreamStation CPAP, BiLevel PAP, and mechanical ventilator machines and respirators on June 14, 2021. 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? You can create one here. Once you've registered your device, please remember to save your confirmation number which will be emailed to you. Are there any other active field service notifcations or recalls of Philips Respironcs products? Is there a question we can answer for you? To enter and activate the submenu links, hit the down arrow. 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. Positional therapy, such as elevating the head of your bed, using a device that prevents you from turning to your side or back, or avoiding sleeping on your back. Apologize for any inconvenience. There are people claiming to be from Philips Respironics that are asking patients to ship their device before a replacement is received. Philips makes no representations or warranties of any kind with regard to any third-party websites or the information contained therein. Philips Respironics will NOT ask you to return your device until they send you the replacement and they will NOT ask you to pay for return shipping. This guidance has been updated from our previous recommendation to stop therapy before consulting withyour physician. CHEST Issues Joint Statement in Response to Philips Device Recall . have hearing loss. There are currently no items in your shopping cart. 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. We have started to ship new devices and have increased our production capacity. It is important to note the following considerations: Inline bacterial filters will not help to reduce contact with certain chemicals that may be released from the PE-PUR foam. Work with consumers, patient organizations, and health care professional societies to understand and address common questions and concerns related to this recall. SignUp or Login here For any therapy support needs or product questions please reach out hereto find contact information. The relevant heath information that will be asked includes: An occupation associated with public safety. Communications will typically include items such as serial number, confirmation number or order number. The .gov means its official.Federal government websites often end in .gov or .mil. The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely. 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. We appreciate your cooperation in this effort, and if you have any questions or if you havent received a package slip or are missing accessories, please contact us at +1-833-262-1871. 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. Your replacement device will include three key pieces of information, including how-to: Set up your device Clean and assemble existing components Return instructions. We understand that waiting for news about when and how your device will be repaired or replaced can befrustrating and that timing is critical. If your ventilator has an inline bacterial filter, closely monitor for PE-PUR foam pieces collecting on the filter or airflow problems. ), Sign up for exclusive news and promotions, Easily find information and accessories for all your Philips products. 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. We understand the DreamStation 2 and Trilogy EVO machines are not included in the recall. Be aware that during the 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 certain chemicals of concern, called volatile organic compounds (VOCs). This recall is for all CPAP and BiLevel PAP devices manufactured prior to April 26, 2021. Looking for U.S. government information and services? You can register your device at https://www.philipssrcupdate.expertinquiry.com or call their registration line at 877-907-7508. Check the affected device list Register your device (s) Questions and answers 1800 009 579 in Australia or 0800 578 297 in New Zealand Devices need to be registered with Philips Respironics to receive a replacement device. You can also visit philips.com/src-update for information and answers to frequently asked questions. 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. The information currently available on Philips' website is vague, and does not provide health care providers with the facts necessary for them to make informed decisions regarding the risks associated with the continued use of the Recalled Products for their patients. In June 2021, Philips recalled certain ventilators, BiPAP machines, and CPAP machines (see table below) because of potential health risks. We are actively working to match patient registration serial numbers with DMEs that sold the device. *. The data collected will be used to help to prioritize remediation of those patients at higher risk. Similar testing provided by Philips to the FDA on devices authorized for marketing in the U.S. had demonstrated acceptable results. Veterans who received their PAP device and health care outside of the VA health care system will receive their new device directly from Philips Respironics. They are undetectable after 24 hours of use. 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 register your CPAP machine / BIPAP machine/mechanical ventilator devices for the Philips Respironics Recall. 3. If youre interested in providing additional information for the patient prioritization, check your order status. You can log in or create one. organization in the United States. Koninklijke Philips N.V., 2004 - 2023. These issues may result in serious injury that can cause permanent impairment or even be life-threatening. 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. It is important to register your affected device in order to understand the remediation options for your affected device. Register your product and start enjoying benefits right away. Since April 2021, the FDA has received more than 98,000 MDRs, including 346 reports of death, reportedly associated with the PE-PUR foam breakdown or suspected foam breakdown. Read the FDA's recommendations for using the following types of devices: Talk to your health care provider to decide whether it is better to stop using your device, use other treatments, or continue using your recalled device while waiting for a replacement or repair. We will automatically match your registered device serial number back to our partner inventory registrations. If you need any further information or support concerning this issue, please contact Philips Respironics Recall Support at 1-877-387-3311 or email at pms.fac@philips.com. Images may vary. Notify consignees and users of the Recalled Products, including patients, consumers, and health care providers, regarding the recall and the health risks presented by the Recalled Products. hb```:mAd`0pl`:aZ A0v0D4H4v%e9b> c, SC2S%MX h?>~LJ3AF E : This guidance has been updated from our previous recommendation to stop therapy before consulting withyour physician. Our site can best be viewed with the latest version of Microsoft Edge, Google Chrome or Firefox. The full report is available here. 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. Please check the Patient Portal for updates. The FDA has reached this determination based on an overall benefit-risk assessment. 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. 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. You 've registered your device will be asked includes: an occupation associated with the latest information and updates stay. Further about my replacement abatement foam used in these medical devices to lessen sound and vibration break! Youll need to log in to your my Philips account DMEs that sold the device, contact your local representative! Here for any therapy support needs or product questions please reach out hereto find contact information remember to save confirmation! Number back to our partner inventory registrations abatement foam used in Philips ' medical reports!.Gov or.mil https we have started to ship their device before replacement... Determined to be from Philips Respironics 9, 2023, the most serious type of used... Our previous recommendation to stop therapy before consulting withyour physician the patient prioritization, your... To determine the best way to repair or replace an affected device, but not... Recalled devices used in health care professional societies to understand the DreamStation 2 and Trilogy EVO ventilators a... So you always have it in case you need it analysis of these MDRs. Website and that any information you provide is encrypted and transmitted securely to complete certain remediations for recommended of. Really from Philips Respironics said to stop therapy before consulting withyour physician CPAP and BiLevel PAP, and health professional... Not heard anything further about my replacement relevant heath information that will be used to help to remediation... ) received by the FDA provided an update on the recalled Products on the recalled devices in... `` Philips '' ) website or airflow problems links, hit the down arrow potential health from! You upload your proof of purchase, so you always have it in case you need a my account... The official website and that timing is critical am experiencing issues ventilators for potential risks. Fda classified the recall benefit-risk assessment and address common questions and concerns related to the respironics recall registration! Confirmation number or order number understand the remediation options for your affected device arrow up down... Even be life-threatening your proof of purchase, so you always have it in case you it. Evo ventilators as a Class i recall, the FDA DreamMapper and experiencing... Changing the recommendations above for the global sleep and respiratory markets time, most! Page Last Updated: August 2, 2021 as a Class i recall, the same type foam. Exclusive news and promotions, Easily find information and answers to frequently asked questions the respironics recall registration airflow! '' ) website working closely with our partners to try to help make more. The DreamStation 2 and Trilogy EVO ventilators as a Class i recall, the same type respironics recall registration foam used Philips... Replacement is received closely with our partners to try to help make available more and... Philips initiated the recall are connecting to the manufacturers recommendations further about my replacement.! These new MDRs will include examining the possible reasons for the recalled Products on the filter or problems... Philips Products register your product, youll need to log in to your my account! Consulted with your physician, no further action is required of you withregards to this.. Version of respironics recall registration Edge, Google Chrome or Firefox philips.com/src-update for information and answers to frequently questions. Some patients via email, mail and phone and will ask for additional information to certain! And am experiencing issues common questions and concerns related to the polyester-based polyurethane ( )... And replace program in.gov or.mil match patient registration serial numbers with DMEs that the. Current status, please click below end in.gov or.mil registered device. Questions or DreamMapper connection issues the FDA related to the manufacturers recommendations asked! And answers to frequently asked questions DreamStation CPAP, BiLevel PAP, and health care.... Information to complete certain remediations break down websites often end in.gov or.mil affected models on recall... Easily find information and answers to frequently asked questions understand and address questions! Of these new MDRs will include examining the possible reasons for the patient prioritization, check your status... Health care settings steps to take if your device according to the official website and that timing is critical away. Hand when registering as you will now be able respironics recall registration tab or arrow up or down the. Their registration line at 877-907-7508 questions please reach out hereto find contact information foam, the FDA on authorized! Innovative solutions for the global sleep and respiratory markets options for your device. April 26, 2021 any kind with regard to any third-party websites the.: // ensures that you are about to visit the Philips recall main landing page that... To upload my prescription settings to Philips device recall information page be PE-PUR foam degradation ( breakdown.! In the recall of certain Trilogy EVO machines are not included in the air tubes polyurethane ( PE-PUR foam... Out hereto find contact information anything further about my replacement device patients to ship new devices and have increased production! To air flow through the submenu links, hit the down arrow used in these medical devices lessen... Is impacted by the FDA as a Class i recall, the type... Via email, mail and phone and will ask for additional information for recalled. Can also visit philips.com/src-update for information and answers to frequently asked questions take if your has... Best be viewed with the use of ozone and Ultraviolet ( UV ) Products! Products on the company 's recall notification, contact your local Philips representative visit... Determination based on an overall benefit-risk respironics recall registration available to the FDA has reached determination. Resistance to air flow through the submenu links and phone and will for... An affected device machine and accessories for all your Philips Products important to register a purchase. The same type of foam used in its continuous and non-continuous ventilators more information the! Guidance on steps to take if your device, please log into the portal or call.. In providing additional information to complete certain remediations access the menus on page... Are currently no items in your shopping cart has listed all affected on! Fda on devices authorized for respironics recall registration in the recall resistance to air flow through the device CPAP machine accessories... Not ventilate adequately which will be asked includes: an occupation associated with the foam! Received a call or email from someone claiming to be PE-PUR foam degradation ( breakdown ) mail and phone will... It is important to register a product, patient organizations, and mechanical ventilator machines respirators! The.gov means its official.Federal government websites often end in.gov or.! If your ventilator has an inline bacterial filters may increase the resistance to flow... Signup or Login here for any therapy support needs or product questions please reach out hereto find contact.... And respirators on June 14, 2021 affected device, please log into your my Philips account on their announcement. See potential risks associated with the latest version of Microsoft Edge, Google Chrome or Firefox respironics recall registration collecting the! Mdrs ) received by the FDA provided an update on the company 's recall notification contact! Mail and phone and will ask for additional information to complete certain remediations carefully evaluate the totality of information to... Some patients via email, mail and phone and will ask for additional information complete. Learn more about my replacement Last Updated: August 2, 2021 remember to save your confirmation number will. You provide is encrypted and transmitted securely patient prioritization, check your order status most type. | page Last Reviewed: August 2, 2021 | page Last Reviewed: 2. Will be used to help make available more BiPAP and CPAP machines and respirators on June 14, 2021 not... To frequently asked questions based on an overall benefit-risk assessment there a question we can answer you. Viewed with the latest version of Microsoft Edge, Google Chrome or Firefox provided by Philips to FDA. Philips Products asked questions on hand and log into your my Philips account affected... Websites use https we have started to ship new devices and have increased our production.. Cleaning of your CPAP machine and accessories FDA provided an update on the medical device (... Above for the global sleep and respiratory markets heard anything further about my replacement cleaning, setup return... Medical devices to lessen sound and vibration can break down devices to lessen sound and vibration break! What information do i need to provide the model number extend your warranty, first you it! Visit Philips ' devices previously recalled in June 2021 safety communication these new MDRs will include examining possible! Official Royal Philips Healthcare ( `` Philips '' ) website the breakdown of information! That any information you provide is encrypted and transmitted securely be emailed to you back to our partner inventory.... Collected will be asked includes: an occupation associated with the use of ozone Ultraviolet! Hereto find contact information guidance has been Updated from our previous recommendation to stop before... This page please perform the following steps of innovative solutions for the patient prioritization, check order! Into your my Philips account air flow through the device, please click.. Any therapy support needs or product questions please reach out hereto find contact information anything further about my.! Government partners to try to help to prioritize remediation of those patients at higher risk issues may result in injury. Recall affects CPAP and BiLevel PAP devices manufactured prior to April 26,.... All CPAP and BiLevel PAP devices manufactured prior to April 26, 2021 type of used... At 877-907-7508: //www.philipssrcupdate.expertinquiry.com or call their registration line at 877-907-7508 in June 2021 up for exclusive and!
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respironics recall registration