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The settlement benefits device users who purchased, leased, rented, paid for or were prescribed a recalled Philips CPAP, Bi-Pap, ventilator or other recalled device. The settlement also benefits insurers, self-funded employers and other third-party payers who reimbursed whole or in part the purchase, lease, rental or other payment for a recalled Philips CPAP, Bi-Pap, ventilator or other recalled device. The settlement also benefits insurers, self-funded employers and other third-party payers who reimbursed whole or in part the purchase, lease, rental or other payment for a Philips CPAP, Bi-Pap, ventilator or other device that was included in a recall. The foam allegedly exposed patients to dangerous chemicals. Payers can receive a payer award depending on the number of insured lives they cover and the amount in premiums they received in the and calendar years. Users who return their recalled device using a prepaid label provided by the settlement will automatically receive a settlement payment. All other class members must submit a valid claim form by Aug.

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We are focused on delivering the best care possible, while supporting patients, customers and clinicians throughout the remediation process. As the remediation of the ventilator devices continues, Philips Respironics will be communicating with Durable Medical Equipment providers DMEs directly throughout the process. If you are a patient or caregiver with an affected Philips Respironics ventilation device, you do not need to take any action. All ventilation remediation will be handled via your DME. September 27, Philips has reached an agreement, subject to final Court approval, to resolve all economic loss claims brought by private plaintiffs in the United States related to the Philips Respironics voluntary recall of certain sleep and respiratory care devices. All related inquiries should be directed to the third-party Settlement Administrator, Angeion Group. For more information, please visit www. Emergency Use Authorization. In-Lab Titration Device. If your device is affected Products that are not affected may have different sound abatement foam materials, as new materials and technologies are available over time.

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We are focused on delivering the best care possible, while supporting patients, customers and clinicians throughout the remediation process. As the remediation of the ventilator devices continues, Philips Respironics will be communicating with Durable Medical Equipment providers DMEs directly throughout the process. If you are a patient or caregiver with an affected Philips Respironics ventilation device, you do not need to take any action. All ventilation remediation will be handled via your DME. September 27,

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Claim Form. The machine may or may not have contributed to his death. AARP Membership. Top Class Actions Legal Statement. Sign up for our free newsletter. We thank you for your patience as we work to restore your trust. Driver Safety. Please be assured that we are working hard to resolve the issue as quickly as possible. Please be assured that we are doing all we can to meet demand, including increasing the production of repair kits and replacement devices. Please be assured that we are doing all we can to resolve the issue as quickly as possible.

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Your Personalized Guide to Fitness. Further testing and analysis on other devices is ongoing. At the time the field safety notice was issued, Philips Respironics relied on an initial, limited data set and toxicological risk assessment. DreamStation 2. Life Balance. Privacy Policy. Small Business. All related inquiries should be directed to the third-party Settlement Administrator, Angeion Group. Leave a Reply Cancel reply Your email address will not be published. Can I buy one and install it instead of returning my device? The foam that is used in some devices to reduce sound and vibration showed signs of degradation damage and chemical emissions.