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  2. Contact and support for Philips Respironics voluntary recall. Voluntary Recall Information. Philips Respironics Sleep and Respiratory Care devices. Contact and support options for patients impacted by the June 2021 voluntary recall of certain CPAP, BiPAP and mechanical ventilators related to PE-PUR sound abatement foam.

  3. May 13, 2024 · Contact Information Customers in the U.S. with questions about this recall should contact Philips Respironics at 1-800-345‐6443 for homecare customers or 1-800-722‐9377 for hospital...

  4. Oct 4, 2022 · 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. In the US, the recall notification has been classified by the FDA as a Class I recall. Devices authorized for repair and replacement include DreamStation CPAP and BiLevel devices, DreamStation ASV ...

  5. We may request contact information or current device settings. Communications will typically include items such as your serial number. If we have attempted to reach you through multiple avenues the request may appear very generic in nature and will contain a Philips customer service number.

  6. If you need any further information or support concerning this recall/issue, please contact the recall support hotline or visit the website: 1-877-907-7508 www.philips.com/src-update.

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  7. that do not involve reported serious injury or death. Philips Respironics provided test result updates on December 23, 2021, June 28, 2022, December 21, 2022, May 16, 2023, and on July 24, 2023. Based on the comprehensive testing and analysis that has been conducted, Philips Respironics concluded that use of its sleep therapy devices is not

  8. Your replacement device will include three key pieces of information, including how-to: Set up your device. Clean and assemble existing components. Return instructions. If you need more information, scan the QR codes and call our support team at +1-833-262-1871 with any questions. 7. Returning your affected device.

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