I just found out yesterday that on 06/14/21 Philips has issued a massive recall of all the Respironics Cpap, Bipap machines and mechanical ventilators manufacturered prior to 04/26/2021 due to potential health risks related to the sound abatement foam used in these devices. For patients using the cpap/bipap machines it is recommended to stop using the machines. I have been been using a bipap machine for 22 years and am currently using one of the affected machines since 2018. I called the home healthcare place where I bought the machine. They knew of the recall and advised me to stop using the machine especially if I have been using a cpap cleaning device that uses ozone e.g. the SoClean device, as the ozone reacts with the sound abatement foam giving off deadly fumes. And of course I have also been using the SoClean device since 2018. Because I have severe sleep apnea, it is impossible for me to sleep without using the machine so I will have to continue to use it as it is unknown at this time when Philips will be able to provide repairs to the machines and/or provide replacement machines. They advised I stop using the SoClean machine. Some of the health risks possible are sore eyes, throat, chest, asthma and possibly even cancer. You can go to the website linked below for more information. You can also input the serial number of your machine and it will indicate whether the machine is affected by the recall. If it is, then you can fill out the form and Philips will contact you when they can repair/relace your machine.
Gary
www.philips.com
Gary

Medical Device Recall Information - Philips Respironics Sleep and Respiratory Care devices
In June 2021, after discovering a potential health risk related to a part in certain CPAP, BiPAP and Mechanical Ventilator devices, Philips issued a voluntary Field Safety Notice (outside U.S.) / voluntary recall notification (U.S. only).
