Philips Respironics Recall

The Philips devices recall affects BiLevel Positive Airway Pressure (BiPAP) devices, Continuous Positive Airway Pressure (CPAP) devices and Mechanical Ventilators manufactured between November 2009 and April 2021, specifically those in the C-Series and all DreamStation 1 platforms.

The recalled machines were made with a type of foam that may degrade over time and release carcinogens that could be inhaled by the user. There was no malfunction detected in the majority of the machines. The foam degradation, which can break down into black debris, may be accelerated in environments with high heat and high humidity.

The company said it would either replace or repair the affected devices within 1 year. In the meantime, some people are being advised to stop using their Philips breathing devices and opt for an alternative.. Other people are being advised to continue use of the devices, as the benefits outweigh the potential risks.

If you have been affected by this recall, it is important to check in with your doctor before completely discontinuing use of your device — especially if you have not yet obtained an alternative.

Please visit thePhilips Respironics Medical Device Recall Notification's Websitefor more details.

To help you determine whether your device is affected by the recall, find your device’s serial number and use the device identification tool provided online byPhilips Respironics Medical Device Recall Notification's list of affected device website page.