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Alternative Treatments for Obstructive Sleep Apnea All CPAP devices run on their own algorithms and have different components so there may still be a period of acclimation when switching CPAP machines. If you like the way your current CPAP device feels, this may be the easiest transition. If you switch to a different CPAP machine, you may be able to keep the same user interface that you are used to. If the risks of your affected machine outweigh the benefits, your physician may recommend that you switch to a different CPAP machine or an alternative treatment to your OSA. Please refer to the following website from Philips to review specific instructions related to the recall: The FDA advises you to keep using your device until your physician decides the benefits do not outweigh the risks. with DreamStation 2 CPAP devices…and intends to complete the repair and replacement programs within approximately 12 months.” What to Do if Philips Recalled Your CPAP Machine
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“…the company has already started replacing certain affected first-generation DreamStation CPAP devices in the U.S. “Philips anticipates reworking to commence in the course of September 2021,” according to Philips Respironics. On September 1, 2021, Philips announced their plans for repairing and replacing affected devices. Get a complete list of all recalled CPAP, BiPAP, and ventilator machines on the FDA’s website. The Philips CPAP recall, issued on June 30, 2021, includes CPAP devices manufactured between 2009 and April 26, 2021.
Philips recalls cpap machines skin#
Other possible adverse reactions from chemical exposure include dizziness, headache, skin and respiratory tract irritation, nausea, vomiting, and carcinogenic effects. Other possible adverse effects from debris exposure include inflammatory response, asthma, carcinogenic effects, and adverse effects to the liver, kidneys, and other organs. Reports of cough, chest pressure, headaches, sinus infections, and upper airway irritation were reported. The air pathway includes the tubing, humidifier, and mask. Philips has received complaints of particles and debris found in the air pathway of affected devices. Adverse Reactions and Consumer Complaints The person using the CPAP will potentially breathe in or swallow chemicals or debris from the PE-PUR foam, which has the potential to cause serious health consequences and could be life-threatening.
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The PE-PUR foam might also give off harmful chemicals in the form of a gas. In these affected devices, the foam might break down, allowing particles to enter the air pathway of the device. In the recalled products, Philips used a sound-diminishing foam that was polyester-based polyurethane-based and known as PE-PUR. The Philips CPAP recall is a Class I recall, the most severe kind, so it is essential to take it seriously. Philips CPAP Recall Facts, Questions, and Answers If your CPAP device made the recall list, read on to learn more about this recall and available alternatives to treat your obstructive sleep apnea (OSA). In 2021, Philips voluntarily recalled certain CPAP, BiPAP, and ventilator machines, leaving consumers with questions.