Once all accessories have been installed, plug in your device to a working wall outlet and wait five minutes for your device settings to upload. Alongside this, we have expanded our pool of experts in the areas of treatment and components, including specialists in toxicology, biocompatability and chemistry. Our update in November 2021 provides broadened guidance regarding affected CPAP, BiLevel PAP and Mechanical Ventilator devices, and mechanical ventilators, as follows: For patients using BiLevel PAP and CPAP devices, talk to a health care provider to decide on a suitable treatment for medical conditions, which may include: Using another similar device that is not part of the recall. Owners or users of DreamStation 1 devices who wish to preserve their units for purposes of a lawsuit have the option of requesting preservation, either by Philips Respironics or by the user, through the Preservation Registry established by Philips Respironics. Also, be sure to keep all packaging materials, as they will be used to return your affected device back to Philips Respironics. Whether in the judgement of the treating clinical team the benefit of continued usage of these ventilator devices may outweigh the potential risks identified in the recall notification. Using packing tape supplied, close your box, and seal it. As part of our commitment to quality and patient safety, Philips Respironics is dedicated to removing product containing the affected sound abatement foam from the market. It is important that you do not stop using your device without discussing with your doctor. All oxygen concentrators, respiratory drug delivery products, airway clearance products. The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely. We are focused on making sure patients and their clinicians have all the information they need. I have been waiting for the replacement of my CPAP and no one has ever contacted me or email. Our physicians have had many meetings with the manufacturer as well as with other sleep medicine practices, and we currently recommend the following: Call Philips Respironics at 1-877-907-7508 to register your device or register your device via the web at: https://www.philipssrcupdate.expertinquiry.com/ Patients who are concerned should check to see if their device is affected. CPAP machines: Tips for avoiding 10 common problems - Mayo Clinic
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