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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
      Remediation progress updates
      Product notification
      Informational webpage icon
      Article
      Learn more about your replacement device
      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