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Philips reaches compliance agreement with FDA over ventilator recall

AMSTERDAM (Reuters) -Dutch health technology company Philips will not sell new devices to treat sleep apnea in the U.S. in the coming years as it works to comply with a settlement with the Food and Drug Administration (FDA) announced on Monday. The agreement followed the recall of millions of breathing devices and ventilators used to treat sleep apnea in 2021 because of concerns that foam used to reduce noise from the devices could degrade and become toxic, carrying potential cancer risks. Phi...
Noord Holland Roy Jakobs Edmund Klamann Shri Navaratnam Bart Meijer Drug Administration Executive Roy Jakobs
Source: yahoo.com

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Philips Q4 Income From Opns Down; To Halt Sleep Devices Sale In US; Stock Dips

Shares of Philips Electronics NV were losing more than 6 percent in the morning trading in Amsterdam as well as in pre-market activity on the NYSE after the Dutch consumer electronics giant reported Monday a drop in fourth-quarter income from operations amid weak sales.
Noord Holland United States Philips Respironics Drug Administration Philips Electronics Us Department Of Justice

Philips stops selling sleep devices in US amid recall woes

Under-fire Dutch medical device maker Philips said Monday it would halt new sales of sleep machines in the United States after a series of recalls that continued to weigh on results. "Until the relevant requirements of the consent decree are met, Philips Respironics will not sell new... sleep therapy devices or other respiratory care devices in the US," the company said.
Noord Brabant Noord Holland United States Philips Respironics Roy Jakobs Drug Administration
Source: tuko.co.ke

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