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Integration of bluetooth technology has allowed Philips Respironics to develop a free App which works alongside the Philips Respironics DreamStation machine. This humidifier also has Dry Box technology, meaning it's much less likely for water to enter the machine through the humidifier unit. The tank is easily removed from the DreamStation Auto CPAP machine and features an open top for convenient cleaning. Philips Respironics have designed the new humidifier with ease of use in mind. The screen is now front facing and a larger size making it easier for patients to make changes or view their data. Improving on an already popular design, the Philips Respironics DreamStation Auto CPAP machine can still be split from the Humidifier to become even smaller for travel purposes. The new DreamStation Auto CPAP machine by Philips Respironics is smaller, lighter and smarter than its predecessor the 60 series. Product: Dreamstation Auto CPAP machine.Philips recall contact number: 1800 830 517 FOR MORE INFORMATION PLEASE FOLLOW LINK BELOW You can contact Philips at (877) 907-7508 for additional help.DUE TO THE PHILIPS PRODUCT RECALL, WE HAVE SUSPENDED SALES OF THIS ITEM.
#Philips dreamstation registration
It also will guide you through the registration process.
#Philips dreamstation how to
The website will give you instructions on how to locate the serial number of your device. To confirm that your Philips PAP device has been recalled, you need to visit the Philips registration site to register your device. Philips noted that it intends to complete the repair and replacement programs within approximately 12 months. The company also is replacing some DreamStation CPAP devices with DreamStation 2 devices. The sound abatement foam in recalled devices will be replaced with a new material. 1, Philips announced that it had received authorization from the FDA to begin its repair and replacement programs for recalled devices. The updated recall notification advises patients using bi-level PAP and CPAP devices to consult with their physician on a suitable treatment plan. Patients, physicians and durable medical equipment (DME) suppliers can call Philips at 87 for additional support. In November 2021, Philips updated the guidance in its recall notification to align with recommendations in an FDA safety communication. High heat and high humidity environments also may contribute to foam degradation.
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Philips indicates that this foam degradation may be exacerbated by use of unapproved cleaning methods, such as ozone. The foam also may off-gas certain chemicals. Potential risks include headache and respiratory problems. The risks include that the foam may degrade into particles, which may enter the device’s air pathway and be ingested or inhaled by the user. However, Philips determined based on testing that there are possible risks to users related to the type of foam used in these devices. Philips reports that it has received a low complaint rate (0.03% in 2020). The AASM also offers guidance for patients and FAQs for patients on the Sleep Education website.Clinicians can view the AASM guidance in response to Philips recall of PAP devices for additional information.Read the Philips press release for more information. The majority of the affected devices are in the first-generation DreamStation product family. The recall is in response to potential health risks related to the sound abatement foam component in these devices. On June 14, Philips issued a recall notification for specific Philips bi-level positive airway pressure (bi-level PAP), continuous positive airway pressure (CPAP), and mechanical ventilator devices. Young Investigators Research Forum (YIRF).Accredited Sleep Technologist Education Program (A-STEP).Advanced Practice Registered Nurses and Physician Assistants (APRN PA).