For patients with an Android (Android version 7 or higher required) or Apple (iOS version 10 or higher required) mobile device, please download the DreamMapper mobile app from your respective app store. We understand the profound impact this recall has had on you, and that for those who are waiting for a repaired or replaced device, this progress cant come quickly enough. Success. Philips Respironics received authorization from the U.S. Food and Drug Administration (FDA) to restore affected first-generation DreamStation devices by replacing the PE-PUR sound abatement foam with a new material. Please note that it is important that you only use approved cleaning methods for our devices and masks, as, We know how important it is to feel confident that your therapy device is safe to use. Register your device on the Philips recall website or call 1-877-907-7508. As part of the remediation process, customers and patients will be provided with more information on the next steps to implement the permanent solution as it becomes available. Koninklijke Philips N.V., 2004 - 2023. Create a new password following the password guidelines. As we have previously noted in connection with the return of your DreamStation device, we will not be returning DreamStation devices back to the original user. Agree This is a potential risk to health. Not all details of this recall are known at this time. Advisory - Philips Respironics recalls several models of CPAP and Our site can best be viewed with the latest version of Microsoft Edge, Google Chrome or Firefox. All rights reserved. If you had a CPAP machine before you got Medicare, you will need to check with Medicare to see if you qualify for certain requirements that will cover the cost of the replacement of your machine. Our update in November 2021 provides broadened guidance regarding affected CPAP, BiLevel PAP and Mechanical Ventilator devices, and mechanical ventilators, as follows: For patients using BiLevel PAP and CPAP devices, talk to a health care provider to decide on a suitable treatment for medical conditions, which may include: Stopping use of an affected device Using another similar device that is not part of the recall Continuing to use an affected device, if a patients health care provider determines that the benefits outweigh the risks identified in the recall notification. We agree. Koninklijke Philips N.V., 2004 - 2023. As new information and options become available to help our customers we will switch our operations accordingly. You can log in or create one here. Philips Sleep and Respiratory Care Devices - Australia and New Zealand Register your device On April 26, 2021, Philips globally provided an important update to the market regarding proactive efforts to address identified issues with a component in certain products of our Sleep & Respiratory Care portfolio. Our update in November 2021 provides broadened guidance regarding affected CPAP, BiLevel PAP and Mechanical Ventilator devices, and mechanical ventilators, as follows: For patients using BiLevel PAP and CPAP devices, talk to a health care provider to decide on a suitable treatment for medical conditions, which may include: Using another similar device that is not part of the recall. UPDATE: Certain Philips Respironics Ventilators, BiPAP Machines, and The foam that is used in some devices to reduce sound and vibration showed signs of degradation (damage) and chemical emissions.
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