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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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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