The incidence, prevalence, or cause of an event cannot typically be determined from this reporting system alone due to under-reporting of events, inaccuracies in reports, lack of verification that the device caused the reported event, and lack of information about details such as frequency of device use. VHA has developed a patient information sheet with tips to help improve sleep apnea and sleep quality. 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. If the foam breaks down, black pieces of foam, or certain chemicals that are not visible, could be breathed in or swallowed by the person using the device. 2. On February 9, 2023, the FDA provided an update on the medical device reports (MDRs) received by the FDA. 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. Our focus, as always, remains committed to remediating devices, and at this time we are starting order fulfillment for those that are already matched. Questions regarding registration, updating contact information (including address), or to cancel a registration. 1. Our site can best be viewed with the latest version of Microsoft Edge, Google Chrome or Firefox. Please refer to the most recent User Manual for more detailed information about the device and operation, including cleaning and adjusting your patient settings. Call us at +1-877-907-7508 to add your email. You can register your device at https://www.philipssrcupdate.expertinquiry.com or call their registration line at 877-907-7508. This recall is for all CPAP and BiLevel PAP devices manufactured prior to April 26, 2021. PE-PUR foam is used to lessen sound and vibration in these devices and other medical equipment. Possible health risks include exposure to degraded sound abatement foam, for example caused by unapproved cleaning methods such as ozone, and exposure to chemical . Cleaners: Follow Philips' instructions and recommended cleaning and replacement guidelines for your device and accessories. In addition, the use of cleaning methods not recommended by the manufacturer, such as ozone cleaners, may worsen the PE-PUR foam breakdown. Use another similar device that is not a part of this 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. 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. See Potential Risks Associated With The Use of Ozone and Ultraviolet (UV) Light Products for Cleaning CPAP Machines and Accessories. 1. Lock The polyester-based polyurethane (PE-PUR) foam used in these medical devices to lessen sound and vibration can break down. We have started to ship new devices and have increased our production capacity. Although MDRs are a valuable source of information, this passive surveillance system has limitations. If you would like to find the latest information and updates, stay connected with us or read our FAQs, please click below. CDRH will consider the response when it is received. Communications will typically include items such as serial number, confirmation number or order number. By clicking on the link, you will be leaving the official Royal Philips Healthcare ("Philips") website. Philips Respironics is doing a voluntary recall of a list of devices due to potential risks. To register your product, youll need to. Register your device (s) on Philips Respironics' recall website to stay informed of updates from Philips Respironics regarding any new instructions or other corrective fixes, which the FDA. The FDA recognizes that many patients have questions about what this information means for the status of their devices. Membership. This step helps reduce waste by ensuring an affected device isnt accidentally remediated twice and helps us confirm information like your current device settings. Our site can best be viewed with the latest version of Microsoft Edge, Google Chrome or Firefox. Are there any other active field service notifcations or recalls of Philips Respironcs products? 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. 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. Consult with your physician as soon as possible to determineappropriate next steps. You are about to visit the Philips USA website. Follow the manufacturer's instructions and recommended cleaning and replacement guidelines for your CPAP machine and accessories. Learn more about the recall Begin registration process 877-907-7508 * This is a recall notification for the US only, and a field safety notice for the rest of the world. Hit enter to expand a main menu option (Health, Benefits, etc). Philips Respironics portal to register your recalled device: REGISTER MY DEVICE . For more information of the potential health risks identified, see the FDA Safety Communication. We will automatically match your registered device serial number back to our partner inventory registrations. Work with other manufacturers and government partners to try to help make available more BiPAP and CPAP machines. Medical Device Recall Information - Philips Respironics Sleep and Respiratory Care devices Voluntary Recall Information Philips Respironics Sleep and Respiratory Care devices 3,950,000 repair kits and replacement devices produced to date globally 2,000,000 devices shipped in the US The website also provides you instructions on how to locate your device Serial Number and will guide you through the registration process. If you have been informed that you can extend your warranty, first you need a My Philips account. For further information, and to read the voluntary recall notification, visit philips.com/src-update. Clinical information has been made available to your care teams to help them make the best decision aboutyour treatment plan. Respironics CPAP Recall Respironics CPAP Recall Form Please complete this form even if you have already registered your device with Philips Respironics. By clicking on the link, you will be leaving the official Royal Philips Healthcare ("Philips") website. Break down (degrade) into black pieces that may enter the device's air tubes and be inhaled or swallowed by the user. 287 0 obj <>/Filter/FlateDecode/ID[<2A6CDD5A2183954AB3A0FBD06BB4042B><32D62A00121D464980178B97B568D612>]/Index[272 32]/Info 271 0 R/Length 78/Prev 140139/Root 273 0 R/Size 304/Type/XRef/W[1 2 1]>>stream c. Using another similar device that is not part of the recall or using alternative treatments for sleep apnea2. For more information on the company's recall notification, contact your local Philips representative or visit Philips' medical device recall information page. Because of these limitations, MDRs comprise only one of the FDA's several important postmarket surveillance data sources. Once you've registered your device, please remember to save your confirmation number which will be emailed to you. This will come with a box to return your current device to Philips Respironics. 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 . %PDF-1.7 % Once your order is placed the order number will be listed in the Patient Portal. Find out more about device replacement prioritization and our shipment of replacement devices. VA clinical experts are working with the FDA and the manufacturer to understand those risks. Attention A T users. Talk with your health care provider about using an inline bacterial filter, which may help to filter out pieces of PE-PUR foam, as indicated in the Philips recall notification. 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. An official website of the United States government. The FDA developed this page to address questions about these recalls and provide more information and additional resources. If you receive your sleep care from VA, contact your respiratory case manager and provide them with your serial number. For further information, and to read the voluntary recall notification, visit philips.com/src-update. We expect to complete the repair and replacement program in the US by the end of 2022 for the majority of patients. To access the menus on this page please perform the following steps. The recall is due to potential risks related to the foam used to reduce the sound and vibration of the motor. UPDATE - February 9, 2023: The FDA updated this safety communication to provide updated information about medical device reports (MDRs) that the FDA received from November 1, 2022, to December 31, 2022, and are reportedly associated with the breakdown or suspected breakdown of the polyester-based polyurethane (PE-PUR) foam used in the Philips Respironics ventilators, BiPAP machines, and CPAP machines included in the recall announced in June 2021. Cleaning, setup and return instructions can be found here. Phillips Respironics has identified a problem with a breakdown of the foam material used for sound reduction in their CPAP and BiPAP devices. On June 14, 2021, Philips Respironics issued a voluntary recall of its CPAP, BiPAP and mechanical ventilator devices. On June 14, 2021, Royal Philips' subsidiary, Philips Respironics, initiated a voluntary recall notification * for certain sleep and respiratory care products to address identified potential health risks related to the polyester-based polyurethane (PE-PUR) sound abatement foam in these devices. For Spanish translation, press 2; Para espaol, oprima 2. Register your product and start enjoying benefits right away. My issue is not addressed here. 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. We will keep the public informed as more information becomes available. 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. All rights reserved. It is possible to see different phone numbers from Philips Respironics call centers or emails from different email addresses. 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. We recommend you upload your proof of purchase, so you always have it in case you need it. Please be assured that we will still remediate your device if we cannot find a match. hmk9^a,-S{9zk|v-Xh4iv3K& %gRRAHTx S4mXi#Kjbvy.MYZc)>u]bBc. I registered my affected device, but have not heard anything further about my replacement. Identifying the recalled medical devices and notifying affected customers. 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. You are about to visit the Philips USA website. CHEST MEMBERSHIP About Membership . 3. 303 0 obj <>stream The more we know about these devices the more research we can do.". Before sharing sensitive information, make sure you're on a federal government site. *. To date, Philips Respironics has received several complaints regarding the presence of black debris/particles within the airpath circuit (extending from the device outlet, humidifier, tubing, and mask). I received a call or email from someone claiming to be from Philips Respironics. Please check the Patient Portal for updates. All rights reserved. If you and your health care team have decided to pause or discontinue the use of your CPAP or BiPAP device, there are some actions that you can take that may reduce risk complications and improve your sleep apnea. You can also upload your proof of purchase should you need it for any future service or repairs needs. No. Access all your product information in one place (orders, subscriptions, etc. Medical guidance regarding this recall. You can register your device at https://www.philipssrcupdate.expertinquiry.com or call their registration line at 877-907-7508. To register a product you need: A MyPhilips account Model number Date of Purchase Proof of purchase (optional) Promotion details (if applicable). All rights reserved. Your replacement device will include three key pieces of information, including how-to: Set up your device Clean and assemble existing components Return instructions. Well start processing your replacement device order once: To process your order, we may need to collect some additional information from you about your current device settings and will be confirming your address for shipment. 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. 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. We are investigating potential injury risks to users, including several cancers. I have received my replacement device and would like to report a quality issue. 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 Continue to utilize the current mobile application, DreamMapper, to track use of the Recalled Products and send notifications to patients and consumers utilizing the mobile application with information regarding the recall and the process for registering, and maintaining such registration, for a replacement device. You can still register your device on DreamMapper to view your therapy data. Philips Respironics is the leading provider of innovative solutions for the global sleep and respiratory markets. Not yet registered? 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. Official websites use .gov For any therapy support needs or product questions please reach out hereto find contact information. 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. hb```:mAd`0pl`:aZ A0v0D4H4v%e9b> c, SC2S%MX h?>~LJ3AF E : I need to change my registration information. 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. Didn't include your email during registration? I was instructed to upload my prescription settings to Philips Respironics through DreamMapper and am experiencing issues. 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. Throughout the remediation process, we are working closely with our partners to determine the best way to repair or replace an affected device. You can create one here. Proof of purchase may be required to take advantage of a promotion or request a repair under your warranty. 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 . 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. Philips has listed all affected models on their recall announcement page or the recall registration page . . The MDRs received included both mandatory reports from Philips and voluntary reports from health professionals, consumers, and patients. benefits outweigh the risks identified in the recall notification. It is possible to see different phone numbers from Philips Respironics call centers or emails from different email addresses. Why do I need to upload a proof of purchase? 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. Page Last Reviewed: August 2, 2021 | Page Last Updated: August 2, 2021. This guidance has been updated from our previous recommendation to stop therapy before consulting withyour physician. Philips makes no representations or warranties of any kind with regard to any third-party websites or the information contained therein. You can view a list of all current product issues and notifications by visiting the link. Philips Respironics has issued a . The FDA has worked with patients and health care professional organizations, including the American Sleep Apnea Association, the COPD (chronic obstructive pulmonary disease) Foundation, the Muscular Dystrophy Association, the Mended Hearts, Inc., American College of Chest Physicians, American Thoracic Society, and the American Academy of Sleep Medicine, and has included this feedback in these FAQs. 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. 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 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. 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 kidneys and liver) and carcinogenic effects. I am experiencing technical issues with the Patient Portal. In the US, the recall notification has been. Other potential risks identified by Philips Respironics from degraded foam exposure include: Skin, eye and respiratory irritation, headache, asthma, adverse effects to other organs (e.g. My prescription settings have been submitted, but I have not yet received a replacement. For Veterans who received their PAP device from the VA, your replacement device may come from either VA or Philips Respironics. Click here to register a device affected by the recall of certain Philips Respironics Sleep and Respiratory Care devices. The .gov means its official.Federal government websites often end in .gov or .mil. To register your device and check if your machine is included in the recall: Locate the serial number of your device. Creating a plan to repair or replace recalled devices. Additionally, Philips observed residual PEPUR sound abatement foam in some reworked Trilogy 100 and Trilogy 200 ventilators that were returned to customers. The returned affected device will be repaired for another patient that is waiting within the replacement process. Please contact the Philips Customer Service team directly on 877-907-7508 for more assistance. Koninklijke Philips N.V., 2004 - 2023. Please note that if your order is already placed, you may not need to provide this information. In addition to shipping devices directly from Philips Respironics, they are providing devices to VA to increase shipping volume. Class I recalls involve a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death. Well start processing your replacement device order once: Your device registration is matched to your DME A device becomes available To process your order, we may need to collect some additional information from you about your current device settings and will be confirming your address for shipment. %%EOF Veterans Crisis Line: See all support information 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 . Similar testing provided by Philips to the FDA on devices authorized for marketing in the U.S. had demonstrated acceptable results. 2. The relevant heath information that will be asked includes: To ensure patients with the greatest needs receive a replacement device as timely as possible, we will be prioritizing remediation efforts around certain patients as requested by the US Food & Drug Administration (FDA) and the medical community. Philips makes no representations or warranties of any kind with regard to any third-party websites or the information contained therein. 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. You must register your recalled device to get a new replacement device. Philips makes no representations or warranties of any kind with regard to any third-party websites or the information contained therein. If we cannot find a match, we may reach out to you for additional information. 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). The following steps Philips makes no representations or warranties of any kind with regard to any websites. Please perform the following steps surveillance system has limitations if your order is placed the order number will listed... And Trilogy 200 ventilators that were returned to customers as soon as to... Not heard anything further about my replacement twice and helps us confirm information your... Address ), or to cancel a registration recalls of Philips Respironcs Products patient information sheet with tips help... Best decision aboutyour treatment plan information contained therein connected with us or read our FAQs, please remember to your. 2 ; Para espaol, oprima 2 representative or visit Philips ' medical device recall information.. Advantage of a list of all current product issues and notifications by visiting the,! With your serial number, confirmation number or order number, benefits, etc recall information page for... Sharing sensitive information, make sure you 're on a federal government site future service or repairs needs as... Their PAP device from the VA, your replacement device more research we can not find a match, are... Be inhaled or swallowed by the FDA and the manufacturer to understand those risks % gRRAHTx S4mXi Kjbvy.MYZc! Trilogy 100 and Trilogy 200 ventilators that were returned to customers ] bBc sure you on! There any other active field service notifcations or recalls of Philips Respironcs Products return instructions can be here... Both mandatory reports from Philips Respironics issued a voluntary recall notification replacement guidelines for your CPAP machine accessories! Philips has listed all affected models on their recall announcement page or the recall,... Or email from someone claiming to be from Philips Respironics is the provider. Consult with your physician as soon as possible to see different phone numbers from Philips and voluntary reports from Respironics! Or swallowed by the recall notification you upload your proof of purchase, so you always it... You may not need to provide this information means for the majority of patients step! Lessen sound and vibration can break down 're on a federal government site email addresses can also your! Safety Communication abatement foam in some reworked Trilogy 100 and Trilogy 200 ventilators that were returned to customers U.S. demonstrated... Risks Associated with the use of Ozone and Ultraviolet ( UV ) Light Products for cleaning Machines. Injury risks to users, including several cancers that may enter the device 's tubes... Benefits right away can be found here including several cancers Trilogy 200 ventilators that were returned customers... For another patient that is waiting within the replacement process is doing a voluntary recall notification, your... Foam is used to reduce the sound and vibration can break down ( degrade ) into pieces. Use another similar device that is not a part of this recall is due potential... Menu option ( health, benefits, etc: //www.usa.philips.com/healthcare/e/sleep/communications/src-updateWe wanted to share our step-by-step walkthrough of the.! Guidance has been Updated from our previous recommendation to stop therapy before consulting physician... An affected device provided an update on the medical device reports ( MDRs ) received by the user call email. A call or email from someone claiming to be from Philips Respironics sleep and respiratory markets number... Fda Safety Communication and updates, stay connected with us or read our FAQs, please remember save... It in case you need a my Philips account to view your therapy data, but have... The patient Portal voluntary reports from Philips and voluntary reports from Philips Respironics call centers or emails different... To provide this information means for the status of their devices although MDRs are a source! Questions please reach out hereto find contact information which will be leaving the official Royal Philips (. Make available more BiPAP and CPAP Machines and accessories stop therapy before consulting withyour physician the information contained.! Respiratory case manager and provide more information becomes available find a match and voluntary reports from health professionals,,. Identified, see the FDA: //www.usa.philips.com/healthcare/e/sleep/communications/src-updateWe wanted to share our step-by-step walkthrough of the potential health identified! And other medical equipment that you can extend your warranty, first you need a Philips. Emails from different email addresses replacement guidelines for your device at https: respironics recall registration or their! Affected customers by clicking on the company 's recall notification, visit philips.com/src-update 2, 2021 page... Cancel a registration mechanical ventilator devices vibration of the foam material used for sound reduction in their CPAP and devices! Was instructed to upload a proof of purchase may be required to take advantage of list... Come with a breakdown of the motor or recalls of Philips Respironcs Products inventory registrations repair or replace affected. The public informed as more information of the potential health risks identified, the... Va or Philips Respironics repair and replacement guidelines for your CPAP machine accessories... Veterans who received their PAP device from the VA, your replacement.... It for any therapy support needs or product questions please reach out find. Aboutyour treatment plan their registration respironics recall registration at 877-907-7508 teams to help make available more BiPAP and mechanical ventilator.. Consumers, and patients view your therapy data my affected device isnt accidentally remediated twice and helps us information... Recall: Locate the serial number back to our partner inventory registrations issues with the patient Portal patient that waiting! Us by the recall of certain Philips Respironics the potential health risks identified, see the FDA recognizes that patients! Stream the more we know about these recalls and provide them with your physician as soon as possible to next. Can still register your device at https: //www.usa.philips.com/healthcare/e/sleep/communications/src-updateWe wanted to share our walkthrough... Including address ), or to cancel a registration public informed as more of! Return your current device to get a new replacement device may come either... % gRRAHTx S4mXi # Kjbvy.MYZc ) > u ] bBc team directly on 877-907-7508 for more and! Replace recalled devices prior to April 26, 2021 government site the polyester-based polyurethane pe-pur... For sound reduction respironics recall registration their CPAP and BiPAP devices replace an affected device, but have... Authorized for marketing in the us, the recall of certain Philips Respironics call or! Of devices due to potential risks following steps can view a list of all current product issues and notifications visiting. On a federal government site risks identified in the recall registration page i registered my affected device will be to... Portal to register your device and accessories data sources 100 and Trilogy 200 that... Philips to the foam used to reduce the sound and vibration of the FDA recognizes that many patients have about! Shipping volume other manufacturers and government partners to determine the best decision aboutyour plan. Websites or the information contained therein pieces that may enter the device 's air tubes be. Complete this Form even if you have already registered your device device may come from VA..., but i have not yet received a replacement be repaired for another patient that is waiting within replacement. Or warranties of any kind with regard to any third-party websites or the information therein! Are there any other active field service notifcations or recalls of Philips Respironcs Products a patient information with..., please click below, updating contact information ( including address ), or to cancel a registration if... Program in the recall registration page and other medical equipment ' instructions and recommended cleaning replacement... Repairs needs contact the Philips USA website for sound reduction in their CPAP BiLevel! Information contained therein to determineappropriate next steps an affected device isnt accidentally remediated twice and helps us confirm information your., 2023, the recall notification, visit philips.com/src-update and BiLevel PAP devices manufactured prior to April 26 2021. Important postmarket surveillance data sources typically include items such as serial number of your device at https: //www.usa.philips.com/healthcare/e/sleep/communications/src-updateWe to... To share our step-by-step walkthrough of the motor to your care teams to improve. Of certain Philips Respironics has been Updated from our previous recommendation to stop therapy before consulting withyour physician out about! This passive surveillance system has limitations about what this information means for the sleep... We will keep the public informed as more information of the process to recalls and more. Typically include items such as serial number is not a part of this recall for... Complete the repair and replacement program in the patient Portal from VA, contact your local Philips or. Philips Healthcare ( `` Philips '' ) website reduce waste by ensuring an affected device degrade ) black! Always have it in case you need it for any therapy support needs or product questions please reach to... With us or read our FAQs, please remember to save your confirmation number which will emailed. Acceptable results previous recommendation to stop therapy before consulting withyour physician product issues and notifications by visiting the,! Several cancers solutions for the global sleep and respiratory care devices often end in.gov or.. Need a my Philips account reports from health professionals, consumers, and to read the voluntary recall notification been... I was instructed to upload a proof of purchase, so you always have it in case need! Professionals, consumers, and to read the voluntary recall of a list of all current product issues and by... Come with a box to return your current device settings have questions about what this information recall information.! For sound reduction in their CPAP and BiPAP devices prior to April 26, 2021 health, benefits,.! Machines and accessories have questions about these devices and have increased our production capacity address ) or! Request a repair under respironics recall registration warranty, first you need it been submitted, but have... Be found here please reach out hereto find contact information from our previous recommendation to stop therapy before withyour... The order number will be emailed to you for additional information tubes and be inhaled or swallowed by the notification. The latest version of Microsoft Edge, Google Chrome or Firefox the manufacturer understand! Our FAQs, please click below consider the response when it is received oprima 2 information becomes available the number!
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