philips cpap recall update | Medical Device Recall Information

Keyword	CPC	PCC	Volume	Score	Length of keyword
philips cpap recall update	1.53	0.9	3486	30	26
philips	0.63	0.9	7994	70	7
cpap	1.12	0.8	3444	3	4
recall	1.39	0.6	6336	78	6
update	0.01	0.5	8833	94	6

Keyword	CPC	PCC	Volume	Score
philips cpap recall update	1.53	0.8	625	100
philips cpap recall update 2024	0.2	0.9	3340	76
philips cpap recall update 2022	0.78	0.3	9796	50
philips cpap recall update 2023	0.46	0.9	3701	76
philips cpap recall status update	0.54	0.7	9841	34
philips respironics cpap recall update	0.36	0.4	8157	57
philips cpap recall lawsuit update	0.1	0.4	5772	35
philips cpap recall replacement status update	1.53	0.2	5618	9
philips cpap recall canada update	1.21	1	2162	62
philips cpap machine recall update	0.14	0.4	262	40
latest update on philips cpap recall	0.11	0.5	4654	97

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

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

WEBSep 27, 2023 · Latest updates. 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. Learn more. Explained: The Philips Respironics Consent Decree. April 4, 2024. Learn more.

DA: 91 PA: 37 MOZ Rank: 32

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 airway...

DA: 14 PA: 15 MOZ Rank: 12

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: 69 PA: 43 MOZ Rank: 27

News & updates | Philips
philips.com

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

WEBMay 16, 2023 · 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). News and updates. An update on our progress.

DA: 36 PA: 68 MOZ Rank: 11

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

WEBThe affected CPAP, BiPAP sleep therapy and ventilator devices can be found at www.philips.com/src-update. The CPAP and BiPAP sleep therapy devices represent the vast majority of the registered affected devices globally. Did the first-generation DreamStation devices follow industry standards?

DA: 6 PA: 98 MOZ Rank: 38

Philips Respironics recall notification/field safety notice
philips.com

https://www.philips.com/c-dam/corporate/newscenter/global/standard/resources/healthcare/2023/Julytesting/Respironics-field-action-FAQ-July-24-2023.pdf

WEBIn May 2023, Philips provided an update on the completed set of test results for the CPAP/BiPAP sleep therapy devices under the recall., i.e., first-generation DreamStation, System One and DreamStation Go devices, that was positive and reassuring.

DA: 80 PA: 99 MOZ Rank: 4

FDA Provides Update on Recall of Certain Philips Respironics …
fda.gov

https://www.fda.gov/news-events/press-announcements/fda-provides-update-recall-certain-philips-respironics-breathing-assistance-machines

WEBJun 14, 2021 · Today, the U.S. Food and Drug Administration is providing an update related to the June 14, 2021, recall of certain Philips Respironics ventilators, continuous positive airway pressure...

DA: 79 PA: 56 MOZ Rank: 86

Federal Court Enters Consent Decree Against Philips Respironics
fda.gov

https://www.fda.gov/news-events/press-announcements/federal-court-enters-consent-decree-against-philips-respironics-following-recall-certain-sleep

WEBApr 9, 2024 · The consent decree comes after Philips Respironics recalled certain ventilators, CPAP and BiPAP machines in June 2021 because of potential health risks—impacting 15 million devices worldwide....

DA: 25 PA: 58 MOZ Rank: 36

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

WEBPhilips Respironics is voluntarily recalling the below devices due to two (2) issues related to the polyester-based polyurethane (PE-PUR) sound abatement foam used in Philips Continuous and Non-Continuous Ventilators: 1) PE-PUR foam may degrade into particles which may enter the device’s the air pathway and be ingested or inhaled by the user, an...

DA: 62 PA: 7 MOZ Rank: 81

Recommendations for Recalled Philips Ventilators, BiPAP …
fda.gov

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

DA: 36 PA: 12 MOZ Rank: 12