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  1. 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. Please note, dependent on which customer care team you need to speak with, we may be experiencing a high volume of calls and wait times may be longer than normal.

  2. Sep 27, 2023 · 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 ...

    • How do I contact Philips If I have a recall?1
    • How do I contact Philips If I have a recall?2
    • How do I contact Philips If I have a recall?3
    • How do I contact Philips If I have a recall?4
    • How do I contact Philips If I have a recall?5
  3. 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 ...

  4. Oct 5, 2023 · Philips recalled the following devices made between 2009 and April 26, 2021: A-Series BiPAP A30. A-Series BiPAP A40 (ventilator) A-Series BiPAP Hybrid A30. A-Series BiPAP V30 Auto (ventilator) C ...

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  6. 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.

  7. November 16, 2021. Philips has updated the US recall notification to align with the FDA’s recommendation in connection with these recalls and provide broader guidance on use. Read the updated recall notification. (225.0KB) For patients using BiLevel PAP and CPAP devices, consult with your physician on a suitable treatment plan.

  8. I have questions about the recent Mask with Magnets notification that my DME was unable to answer. 877-387-3311. (M-F 8:30a-5p EST) Contact and support for Philips Respironics voluntary recall.

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