philips respironics cpap recall | Medical Device Recall Information -

Keyword	CPC	PCC	Volume	Score	Length of keyword
philips respironics cpap recall	0.07	0.2	3168	88	31
philips	0.35	0.3	9099	36	7
respironics	1.89	0.9	1404	1	11
cpap	1.61	0.7	9722	60	4
recall	0.09	1	4266	44	6

Keyword	CPC	PCC	Volume	Score
philips respironics cpap recall	1.49	0.1	2080	26
philips respironics cpap recall website	1.6	0.4	7401	57
philips respironics cpap recall update	1.97	0.9	5483	90
philips respironics cpap recall 2021	1.79	0.1	9632	72
philips respironics cpap recall phone number	1.21	0.8	2902	10
philips respironics cpap recall list	0.12	0.5	8975	54
philips respironics cpap recall lawsuit	0.24	0.6	4799	30
philips respironics cpap recall registration	0.64	0.9	4797	82
philips respironics cpap recall status	0.47	0.8	6051	10
philips respironics cpap recall number	0.24	0.9	1883	29
philips cpap machines respironics recall	0.41	0.3	8403	48
philips respironics cpap machine recall	0.26	0.3	5883	84
philips respironics cpap mask recall	0.21	0.3	5646	87
fda recall philips respironics cpap	1.28	0.6	1460	53

Search Results related to philips respironics cpap recall on Search Engine

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

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

WebSep 27, 2023 · 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). We are focused on delivering the …

DA: 23 PA: 82 MOZ Rank: 82

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...

DA: 30 PA: 27 MOZ Rank: 39

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

DA: 62 PA: 42 MOZ Rank: 24

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: 35 PA: 20 MOZ Rank: 53

Explained: The voluntary Philips Respironics sleep and
philips.com

https://www.philips.com/a-w/about/news/src-recall-explained.html

WebIn June 2021, Philips initiated a voluntary recall notification / field safety notice for certain CPAP and BiPAP sleep therapy devices and mechanical ventilators to address potential health risks related to the polyester-based polyurethane (PE-PUR) sound abatement foam in …

DA: 21 PA: 42 MOZ Rank: 35

Philips Respironics Recalls Certain Ventilators, CPAP, and …
fda.gov

https://www.fda.gov/medical-devices/medical-device-recalls/philips-respironics-recalls-certain-continuous-and-non-continuous-ventilators-including-cpap-and

WebOn June 14, 2021, Philips Respironics sent customers an “Urgent: Medical Device Recall” letter requesting them to take the following actions: Discontinue use of the device and work with a...

DA: 85 PA: 63 MOZ Rank: 4

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: 43 PA: 49 MOZ Rank: 92

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?

DA: 61 PA: 39 MOZ Rank: 81

News & updates | Philips
philips.com

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

WebMay 16, 2023 · 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). News and updates.

DA: 96 PA: 13 MOZ Rank: 45

Philips provides update on Respironics recall - News | Philips
philips.com

https://www.philips.com/a-w/about/news/archive/standard/news/press/2023/update-october-2023.html

WebOct 06, 2023. Philips provides update on Respironics recall. Philips’ first priority is the health and well-being of patients, both in terms of providing replacement devices and testing to seek more clarity on the safety of the sleep and respiratory care devices under the recall.

DA: 3 PA: 47 MOZ Rank: 91