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Philips Respironics voluntary field safety notice: news updates
 

This page is intended to provide you with the latest news updates on the Philips Respironics voluntary field safety notice.

Patient safety and quality is our priority

 


We understand how important Philips Respironics sleep and respiratory care devices are to patients who use them. Philips acted to protect patient safety by initiating and executing a voluntary recall/field action of significant scale in June 2021.

Patient safety and quality remains our top priority, and we continue to dedicate all necessary resources to ensure that impacted patients receive remediated devices. Philips regrets any distress and concern this recall has caused patients, their families and care providers. We deeply apologize for this and continue to work hard to resolve this for our patients and customers.

If you are a patient, business customer or a clinician,
please visit this page for more information.

If you are an investor or financial analyst,
please visit this page for more information.

Explained: The voluntary Philips Respironics sleep and respiratory care devices recall*
 

*This is a voluntary recall notification in the US and field safety notice in other countries

Philips Respironics - Update on PE-PUR testing results and conclusions available to
date - Full Report
 

Media contacts

If you are representing media and have a question about Philips, please reach out to our media contact for support.

Steve Klink

Steve Klink

Philips Global Press Office

Tel: +31 6 10888824

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Mario Fante

Mario Fante

Philips Global Press Office

Tel: +1 603 560 9226

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