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(6/18/2021 Update) Concerning the Philips Respironics Recall:

We have received official communication from Philips Respironics (PR) concerning the recall of certain CPAP/BiPAP units. They have a process of reporting and replacing the affected devices.  You can call 1-877-907-7508 or visit the website - philips.com/src-update to see if your device is affected by the recall and what to do to have it replaced. The serial number will be on the underside or back of your device – you will need this to communicate information to Philips Respironics.

Philips Respironics has identified a potential serious problem with many of the respiratory care devices that they have made and are issuing a voluntary recall. The devices that we are concerned with are DreamStation (DS1) CPAP & BiPAPs manufactured prior to April of 2021 (Not the new DreamStation 2) as well as CPAP/BiPAPs of the System One (Q Series model- made just prior to the DS1) going back to 2009. Also, for us, there are a small number of mechanical ventilators that are being recalled as well.

Philips Respironics has recommended that you stop using any recalled devices (not including the life support ventilator devices).  We would advise you to talk with your doctor and weigh the potential risk of interrupting your therapy versus what PR has characterized as a very low risk of your machine producing foam particles or toxic chemicals that would then enter the air stream of breathing. The only cases of this that have been reported or complained of are apparently related to the use of Ozone Cleaning Devices (such as the SoClean). The actual risk that PR has put forward at this time is in the order of 0.03% - that is 3 in 10,000 machines that might be affected. This situation is in development at this time and we will advise you on further action going forward.  For more information please call 1-877-907-7508 or visit the website - philips.com/src-update

 

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