Philips' US sales of sleep apnea devices face years-long halt after FDA
deal
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[January 29, 2024]
By Bart H. Meijer
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.
Philips said it had reached what is known as a consent decree that
spells out the improvements it needs to make at its Respironics plants
in the U.S.
Until the conditions are met, no new Respironics devices will be sold in
the U.S., the company said.
Philips shares traded down 5.2% at 0845 GMT in Amsterdam, after news of
the agreement, which ING analyst Marc Hesselink said was "very
punitive".
"We believe it will be very difficult for Philips to recover its U.S.
Respironics market position," Hesselink said in a note.
The decree is being finalised and will be submitted to the relevant U.S.
court for approval. It was not clear how long that would take.
CEO Roy Jakobs declined to give details on the conditions that Philips
will have to meet, but as a general indication said it on average takes
between five and seven years to comply with consent decrees in the
medical equipment industry.
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The corporate logo of the U.S. Food and Drug Administration (FDA) is
shown in Silver Spring, Maryland, November 4, 2009.REUTERS/Jason
Reed/File Photo
 Philips said the costs of the
agreement led to a provision of 363 million euros ($393.5 million)
in the fourth quarter of last year, and were expected to be about 1%
of total revenues in 2024.
Even after the consent decree, Philips faces numerous cases brought
by patients who say their health has suffered due to the use of the
devices, and the outcome of an investigation by the U.S. Department
of Justice into the handling of the recall.
Philips said the agreement did not change its financial targets for
2025, set out last year.
Due to the provision, Philips core profit in the fourth quarter
remained roughly stable at 653 million euros, while comparable sales
fell 1%.
Analysts in a company-compiled poll on average had predicted
adjusted EBITA would rise to 672 million euros, from 651 million
euros a year before, with comparable sales growth of 2.6%.
($1 = 0.9226 euros)
(Reporting by Bart Meijer; Editing by Edmund Klamann, Shri
Navaratnam and Barbara Lewis)
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