飞利浦在2021年中旬开始召回涉及数百万台CPAP和BiPAP呼吸机及其他呼吸设备。召回原因是这些用于治疗睡眠呼吸暂停的设备中的消音组件有声音消减泡沫，可能会降解并进入气道。目前，飞利浦将支付至少4.79亿美元，以解决召回相关的索赔。 在随后的两年中 ...

The US Food and Drug Administration issued a Class I recall Friday, the most serious type of recall, for certain Philips Respironics DreamStation1 CPAP machines. A Class I recall means the FDA has ...

Get all the latest news on coronavirus and more delivered daily to your inbox. Sign up here. As doctors face a shortage of ventilators that are crucial for treating coronavirus patients with ...

Just a few weeks after racking up its fifth Class I recall from the FDA this year, Philips has hit the half-dozen mark. Its sixth of the classifications—which denote the agency’s most serious rating ...

The trouble seemingly never ends for Philips’ beleaguered Respironics division. Since beginning a recall of around 5.5 million ventilators and other breathing support machines more than a year ago, in ...

The U.S. Food and Drug Administration has updated a recall affecting millions of Philips sleep apnea machines, now saying that they may been linked to at least 561 deaths. The agency, in a statement ...

Operating under the idea that a Constant Positive Airway Pressure (CPAP) machine isn’t very far removed electrically or mechanically from a proper ventilator, [Trammell Hudson] has performed some ...