philips respironics recall website | Medical Device Recall Information

Keyword	CPC	PCC	Volume	Score	Length of keyword
philips respironics recall website	1.94	1	4497	22	34
philips	0.68	0.8	7669	53	7
respironics	0.1	0.4	9439	2	11
recall	1.51	0.6	7059	75	6
website	1.9	0.4	2017	82	7

Keyword	CPC	PCC	Volume	Score
philips respironics recall website	0.78	0.3	2872	67
philips respironics recall website online	0.86	0.1	4386	32
philips respironics cpap recall website	0.64	0.8	2917	49
philips respironics recall website here	0.59	0.7	9502	62

Search Results related to philips respironics recall website on Search Engine

Medical Device Recall Information - Philips Respironics Sleep and
philips.com

https://www.usa.philips.com/healthcare/e/sleep/communications/src-update

WebIn June 2021, after discovering a potential health risk related to the foam in certain CPAP, BiPAP and Mechanical Ventilator devices, Philips Respironics issued a voluntary Field Safety Notice (outside U.S.) / voluntary recall notification (U.S. only).

DA: 33 PA: 48 MOZ Rank: 53

How to return your affected device - Philips
philips.com

https://www.usa.philips.com/healthcare/e/sleep/communications/src-update/news/how-to-return-your-affected-device

WebNov 14, 2022 · Voluntary Recall Information. Philips Respironics Sleep and Respiratory Care devices. News and Updates > How to return your affected device. How to return your affected device. November 14, 2022.

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Contact and support for Philips Respironics voluntary recall
philips.com

https://www.usa.philips.com/healthcare/e/sleep/communications/src-update/contact-and-support

WebContact and support options for patients impacted by the June 2021 voluntary recall of certain CPAP, BiPAP and mechanical ventilators related to PE-PUR sound abatement foam. Please note, dependent on which customer care team you need to speak with, we may be experiencing a high volume of calls and wait times may be longer than normal.

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URGENT: Medical Device Recall - Philips
philips.com

https://www.philips.com/c-dam/b2bhc/master/landing-pages/src/update/documents/philips-recall-letter-2021-05-a-2021-06-a.pdf

WebRegister your device(s) on the recall website www.philips.com/src-update . The website provides you current information on the status of the recall and how to receive permanent corrective action to address the two (2) issues.

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Important update to Philips US recall notification | Philips
philips.com

https://www.usa.philips.com/healthcare/e/sleep/communications/src-update/news/important-update-to-philips-us-recall-notification

WebNovember 16, 2021. Philips has updated the US recall notification to align with the FDA’s recommendation in connection with these recalls and provide broader guidance on use. Read the updated recall notification. (225.0KB) For patients using BiLevel PAP and CPAP devices, consult with your physician on a suitable treatment plan.

DA: 47 PA: 33 MOZ Rank: 20

News & updates | Philips
philips.com

https://www.usa.philips.com/healthcare/e/sleep/communications/src-update/news

WebMay 16, 2023 · Voluntary Recall Information. Philips Respironics Sleep and Respiratory Care devices. In June 2021, after discovering a potential health risk related to the foam in certain CPAP, BiPAP and Mechanical Ventilator devices, Philips Respironics issued a voluntary Field Safety Notice (outside U.S.) / voluntary recall notification (U.S. only).

DA: 55 PA: 70 MOZ Rank: 53

Recalled Philips Ventilators, BiPAP Machines, and CPAP Machines
fda.gov

https://www.fda.gov/medical-devices/respiratory-devices/recalled-philips-ventilators-bipap-machines-and-cpap-machines

WebOct 5, 2023 · In June 2021, Philips Respironics (Philips) recalled certain ventilators, bi-level positive airway pressure (also known as Bilevel PAP, BiPAP, or BPAP) machines, and continuous positive...

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Updates to Questions and Answers | Philips
philips.com

https://www.usa.philips.com/healthcare/e/sleep/communications/src-update/news/update-august-27-2021

WebAug 27, 2021 · Voluntary Recall Information. Philips Respironics Sleep and Respiratory Care devices. If you haven't yet registered your device. Learn more about the recall. Begin registration process. 877-907-7508. News and Updates > Updates to Questions and Answers. Updates to Questions and Answers. August 27, 2021. Is this a recall?

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Tools and resources to support your patients - Philips
philips.com

https://www.usa.philips.com/healthcare/e/sleep/communications/src-update/news/dme-tools-and-resources

WebSep 5, 2023 · Read the FSN recall notification. (225.0KB) Check the affected device list. If your patient’s remediation is being managed by Philips Respironics, we ask that you share the following information with them. Register an affected device and keep patients updated on the status of their replacement device.

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Philips Respironics recall notification/field safety notice
philips.com

https://www.philips.com/c-dam/corporate/newscenter/global/standard/resources/healthcare/2023/respironics-update/respironics-field-action-faq-october-23-2023.pdf

WebPhilips Respironics recall notification/field safety notice* announced on June 14, 2021. Frequently Asked Questions – as of October 23, 2023. General. What is the component quality issue in certain of Philips Respironics sleep and respiratory care products? website

website

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