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US FDA received more than 116,000 MDRs, including 561 reports of death tied to recalled Philips sleep apnea machines (02-02-2024)

Maryland, 2 Feb 2024: The Food and Drug Administration says 561 deaths have been reported in connection to recalled Philips devices to treat obstructive sleep apnea and other breathing disorders.

 

The FDA said that since April 2021 it has received more than ......
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Source : Yahoo News
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