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    1. News
    2. Business Updates
    3. June 2021 recall of certain CPAP BiPAP and Mechanical Ventilator devices

    June 2021 recall of certain CPAP, BiPAP and Mechanical Ventilator devices

    In June 2021, after discovering a potential health risk related to the foam in certain CPAP, BiPAP and Mechanical Ventilator devices, Philips Respironics issued a voluntary Field Safety Notice (outside U.S.) / voluntary recall notification (U.S. only). We are focused on delivering the best care possible, while supporting patients, customers and clinicians throughout the remediation process.

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    6 of 3 results
    Informational webpage icon
    Article
    Learn more about your replacement device
    Product notification
    Informational webpage icon
    Article
    Remediation progress updates
    Product notification
    Informational webpage icon
    Article
    Testing results for devices affected by the June 2021 recall
    Product notification

    Features

    Download the Field Safety Notice

    Review the FSN recall notification including affected devices and actions to be taken.

    Download
    Document with magnifying glass icon
    Ozone cleaner information

    Ozone and UV light cleaning products are not currently approved cleaning methods for sleep apnea devices, ventilators or masks and should not be used.

    Learn more
    Red stop sign
    Recall explained

    Learn why Philips issued the voluntary June 2021 recall and the steps taken to ensure patient safety.

    Learn more
    Man in bed operating CPAP on bedside table