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Philips Agrees to Halt Sales of CPAP Devices in the U.S.

The company recorded a provision of EUR 363 million that relates to remediation activities.

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Philips said it has agreed on the terms of a consent decree with the U.S. Department of Justice. The consent decree primarily focuses on Philips Respironics’ business operations in the U.S.

In the U.S., Philips Respironics will continue to service sleep and respiratory care devices already with healthcare providers and patients, and supply accessories (including patient interfaces), consumables (including patient circuits), and replacement parts (including repair kits). Until the relevant requirements of the consent decree are met, Philips Respironics will not sell new CPAP or BiPAP sleep therapy devices or other respiratory care devices in the U.S.

Outside the U.S., Philips Respironics will continue to provide new sleep and respiratory care devices, accessories (including patient interfaces), consumables (including patient circuits), replacement parts (including repair kits) and services, subject to certain requirements.

As a consequence of addressing this consent decree, which is a multi-year plan, Philips recorded a provision of EUR 363 million in Q4 2023 that relates to remediation activities, inventory write-downs and onerous contract provisions. In 2024, Philips expects around 100 basis points of costs that relate to remediation activities and disgorgement payments for Philips Respironics sales in the U.S.

Further details will become available once the consent decree has been finalized and submitted to the relevant U.S. court for approval.

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