Philips on Monday said it will halt the sales of new sleep-therapy devices in the U.S., as part of a broader settlement that led the company to take a €363 million ($393 million) provision.
Philips said it will not sell any new Continuous Positive Airway Pressure or Bilevel Positive Airway Pressure sleep therapy devices or other respiratory care devices in the U.S., until it meets the requirements of a consent decree with the U.S. Justice Department that is being finalized but will need court approval.
Philips will be able to service existing machines and sell accessories, and the restrictions will not apply outside the U.S.
Philips said the new provision covers remediation activities, inventory write-downs and onerous contract provisions.
Philips has had to recall millions of sleep therapy and respiratory machines because of the risk that the foam used in the devices breaks down and can be swallowed. More recently, the Food and Drug Administration reported the risk of overheating in newer devices.
The settlement terms were released as part of its fourth-quarter financials, in which it swung to a €38 million profit while sales fell 7% to €5.06 billion. On a comparable basis, Philips said sales fell by 1% and orders fell by 3%.
Philips expects to deliver 3% to 5% comparable sales growth and an adjusted EBITA margin between 11% and 11.5% this year, after a 10.5% adjusted EBITA margin excluding provisions in 2023.
Philips shares
PHIA,
PHG,
fell 5% in early Amsterdam trade. The stock has gained 26% over the last 52 weeks.
Analysts at Citi called the fourth-quarter results “mixed” but said the consent decree provides “much-needed clarity.”
