Recall Of Philips CPAP Device Causing Worldwide Shortage Of Devices

The video discusses the challenges faced by patients with obstructive sleep apnea due to a recall of Philips CPAP machines. The recall, caused by potentially harmful foam, has led to significant delays in treatment. The video explains the functionality of CPAP machines and the health risks associated with the recall. It also covers the market impact, including increased costs and demand for machines. The FDA's response and Philips' efforts to address the issue are highlighted, along with alternative treatments and future expectations for resolving the shortage.

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