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FDA Gives ‘Most Severe’ Class I Label To Philips’ Recall Of Faulty Ventilators, Sleep Apnea Machines

FDA Gives 'Most Severe' Class I Label To Philips' Recall Of Faulty Ventilators, Sleep Apnea Machines

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The FDA handed down its Class I label, the most severe recall classification, for Koninklijke Philips NV’s (NYSE:PHG) ventilators for at-home and clinical use after the devices were found to put users at risk of inhaling or swallowing dangerous pieces of debris. Philips initiated the recall in mid-June.

...read full article on Benzinga

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