philips respironics recall | Medical Device Recall Information

Keyword	CPC	PCC	Volume	Score	Length of keyword
philips respironics recall	0.83	0.2	7117	73	26
philips	1.47	0.4	1533	4	7
respironics	0.95	0.8	2845	50	11
recall	1.46	0.2	3215	57	6

Keyword	CPC	PCC	Volume	Score
philips respironics recall	0.64	0.8	6879	10
philips respironics recall website	1.25	1	3982	68
philips respironics recall 2021	0.86	0.6	5930	21
philips respironics recall phone number	1.31	1	1271	87
philips respironics recall list	1.5	0.7	6157	43
philips respironics recall register	0.41	0.9	9584	15
philips respironics recall update	0.6	0.9	2248	81
philips respironics recall patient portal	1.22	0.5	9187	95
philips respironics recall status	1.03	1	2386	27
philips respironics recall lawsuits	1.61	0.8	798	66
philips respironics recall cpap	1.25	0.1	5783	96
philips respironics recall update latest	0.22	0.5	2227	70
philips respironics recall canada	0.85	0.7	3252	81
philips respironics recall claim form	0.01	0.7	7536	94
philips respironics recall 2021 register	0.5	0.2	674	33
philips respironics recall registration form	1.72	0.8	1830	77

Search Results related to philips respironics 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 · 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: 15 PA: 20 MOZ Rank: 11

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: 6 PA: 95 MOZ Rank: 10

UPDATE: Certain Philips Respironics Ventilators, BiPAP …
fda.gov

https://www.fda.gov/medical-devices/safety-communications/update-certain-philips-respironics-ventilators-bipap-machines-and-cpap-machines-recalled-due

WEBThe U.S. Food and Drug Administration (FDA) is updating the June 2021 safety communication about the Philips Respironics (Philips) recalled ventilators, bilevel positive airway pressure...

DA: 19 PA: 1 MOZ Rank: 80

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

WEBTrilogy 100, Trilogy 200, Garbin Plus, Aeris, LifeVent, BiPAP V30, and BiPAP A30/A40 Series Device Models. Philips 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 ...

DA: 54 PA: 72 MOZ Rank: 98

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 with broader guidance on use following discussions with regulatory agencies and further assessment of the affected devices.

DA: 51 PA: 56 MOZ Rank: 48

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: 42 PA: 28 MOZ Rank: 50

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 these devices.

DA: 94 PA: 5 MOZ Rank: 53

Philips Respironics Recalls Certain Ventilators and BiPAP …
fda.gov

https://www.fda.gov/medical-devices/medical-device-recalls/philips-respironics-recalls-certain-ventilators-and-bipap-machines-due-potential-health-risks-pe-pur

WEBThe FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death. Recalled Product. Mechanical ventilation devices:...

DA: 10 PA: 39 MOZ Rank: 97

Philips Respironics Recalls Certain Continuous and Non …
fda.gov

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

WEBPhilips Respironics, Inc., is recalling its Continuous and Non-Continuous Ventilators due to the polyester-based polyurethane (PE-PUR) sound abatement foam, which is used to reduce sound and...

DA: 42 PA: 67 MOZ Rank: 96

Philips Respironics recall notification/field safety notice
philips.com

https://www.philips.com/c-dam/corporate/newscenter/global/standard/resources/healthcare/2023/May16Testing/respironics-field-action-faq.pdf

WEBPhilips Respironics recall notification/field safety notice* announced on June 14, 2021. Frequently Asked Questions – as of May 16, 2023. General. What is the component quality issue in certain of Philips Respironics sleep and respiratory care products?

DA: 45 PA: 78 MOZ Rank: 24