Is Philips EverFlo oxygen concentrator dangerous?

No. The most popular model 5 LPM oxygen concentrator by Philips does not contain the toxic polyurethane foam used in the Philips CPAP, BiPAP and ventilator devices that were recalled.

Is the Philips EverFlo oxygen concentrator recalled?

There is no reason to recall the EverFlo as this oxygen concentrator does not contain the dangerous polyurethane foam that degrades over time, and hence is not dangerous for the user. Philips Respironics recalled its problematic CPAP, BiPAP and ventilator machines. There is no need to worry if you are using a Philips Respironics EverFlo home oxygen system.

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Is the Philips EverFlo Q Oxygen Concentrator recalled by Philips?

News about millions of CPAP, BiPAP and ventilator devices being recalled took the sleep apnea world by a storm, after Philips announced that the majority of their respiratory devices have been found to contain a potentially toxic ingredient. Until the potential health hazard for the users has been resolved, Philips is to withdraw every affected unit from the market, while patients are to contact their doctors and discuss an immediate replacement.

If you want to read more about the news, you can do so here, but today we will answer another important question regarding another bestselling Philips respiratory equipment that is being used by millions of patients worldwide – the Philips Respiraonic EverFlo Q and the EverFlo Oxygen Concentrators. The EverFlo Q is a home oxygen system that has become extremely popular not only in Europe and the US, but also in Asian countries, like India, Sri Lanka, Afghanistan and Nepal, where the third COVID-19 wave infected millions of people.

If you are using a Philips Respironics EverFlo Oxygen Conncetrator 5 LPM at home, then you might have already heard the bad news about the mass recall and now are asking yourself whether the EverFlo is also affected by the recall. This is something you should definitely worry as the toxic material found in some of the most popular CPAP machines and ventilators by Philips is considered potentially toxic to the respiratory system.

So far Philips has not received proof that the problematic polyurethane foam — which, over time, degrades and enters the lungs of the user — has caused cancer to consumers, but the news of the recall — and the reason behind it it — has caused serious concerns among patients using the affected respiratory products by Philips.

Philips EverFlo and EverFlo Q - Oxygen Concentrator Banner - CPAPEuropa

Are oxygen concentrators made by Philips recalled?

No. So far only Philips CPAP, BiPAP and ventilators have been recalled due to the health-hazardous material used in their inner sound-suppressing materials. The oxygen concentrator line by Philips Respironics (including the popular EverFlo and EverFlo Q models) do not use the same toxic-upon-degradation material.

Is the Philips EverFlo Q oxygen concentrator recalled?

No. There is no reason to recall the EverFlo Q or the EverFlo models, as these oxygen concentrators do not contain the dangerous polyurethane foam that degrades over time, and hence are not dangerous for the user. Philips Respironics recalled only its problematic CPAP, BiPAP and ventilator machines. There is no need to worry if you are using a Philips Respironics EverFlo home oxygen system.

Which Philips CPAP machines are being recalled?

The Philips recall affected the most popular Philips CPAP machines, like the DreamStation and the System ONE, which have been used by millions of sleep apnea patients over the globe. See all of the recalled units here.

Which Philips CPAP machines are being recalled?

You may heave heard the big news about Philips recalling its Continuous Positive Airway Pressure (CPAP), Bi-Level Positive Airway Pressure (Bi-Level PAP) and mechanical ventilator devices. The news sent tremors across the sleep apnea community as millions of devices were to announced to be recalled until the potential health hazard for the user has been resolved. The reason for the withdrawal is Philips’ announcement that their CPAP devices and ventilator may be dangerous for the consumers due to a hazardous polyurethane foam in their design that could be toxic when degrading. But which Philips CPAP machines are being recalled — you may be asking yourself this question after hearing the breaking news. In this article will answer the question which CPAP models are being withdrawn and what you should do if you are currently using one of the potentially dangerous machines in 2023.

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Here’s the full list of the withdrawn CPAP, BiPAP and ventilator machines by Philips

The specific Philips Bi-Level Positive Airway Pressure (Bi-Level PAP), Continuous Positive Airway Pressure (CPAP) and mechanical ventilator devices that were recalled and are no longer available for purchase in 2023. The following devices have been listed by Philips as possibly dangerous due to the polyurethane foam used in their design.

All Philips CPAP devices manufactured before April 26, 2021, under all serial numbers, are being recalled.

E30 (Emergency Use Authorization);
SystemOne ASV4;
C Series ASV, S/T, AVAPS;
OmniLab Advanced Plus In-Lab Titration Device;
SystemOne (Q series);
DreamStation ASV;
DreamStation ST, AVAPS;
DreamStation CPAP, Auto CPAP, BiPAP;
DreamStation GO CPAP, APAP;
Dorma 400, 500 CPAP;
REMStar SE Auto CPAP;
Trilogy 100 Ventilator;
Trilogy 200 Ventilator;
Garbin Plus, Aeris, LifeVent Ventilator;
A-Series BiPAP V30 Auto Ventilator.

If you are using one of the above-listed models, you should immediately discontinue use and contact your doctor about replacement CPAP therapy with another machine. If you are using life-sustaining mechanical ventilator, you should not stop using the device without first consulting with your doctor. Your doctor will be able to provide you alternate ventilator options that will sustain the therapy you have been prescribed need without risking your health.

Everything you need to know about the withdrawn ventilators

Here’s what you need to know about the withdrawn models CPAP and ventilators by Philips.

All Philips BiLevel PAP devices manufactured before April 26, 2021, under all serial numbers.

E30 model ventilator

designed for minimum ventilatory support for facility use.

DreamStation

non-life supporting continuous ventilator models ASV, ST, and AVAPS.

SystemOne ASV4

Continuous ventilators, non-life supporting model.

C Series

Continuous ventilator, non-life supporting models ASV, S/T, and AVAPS.

OmniLab Advanced Plus

in-lab titration device.

SystemOne Q

Series models of non-continuous ventilators.

DreamStation CPAP, Auto CPAP, and BiPAP

all ventilator models under all serial numbers.

DreamStation Go CPAP and APAP

all models of non-continuous ventilators.

Dorma 400 and 500

CPAP models of non-continuous ventilators.

REMStar SE Auto

CPAP models of non-continuous ventilators

The Trilogy 100, Trilogy 200, Garbin Plus, Aeris, and LifeVent

Continuous ventilators.

The A-Series BiPAP V30 Auto and Hybrid A30

continuous ventilators for minimum ventilatory support for facility use.

Outside the United States, the A-Series BiPAP A30 and A40

Non-life supporting continuous ventilators.

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Is Philips EverFlo Q oxygen concentrator recalled by Philips?

Is the Philips EverFlo Q Oxygen Concentrator recalled by Philips?

Are oxygen concentrators made by Philips recalled?

Is Philips EverFlo oxygen concentrator dangerous?

Is the Philips EverFlo Q oxygen concentrator recalled?

Which Philips CPAP machines are being recalled?

Which Philips CPAP machines are being recalled?

Which Philips CPAP machines are being recalled?

Here’s the full list of the withdrawn CPAP, BiPAP and ventilator machines by Philips

Everything you need to know about the withdrawn ventilators

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