Which Philips CPAP machines are being recalled?

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 In this article will answer the question which CPAP models are being withdrawn and what you should do if you are currently using one of the potentially dangerous machines in 2023.

Looking for a brand new and cheap replacement CPAP that is NOT manufactured by Philips and is 100% safe? No problem.

Check out the best budget-friendly CPAP machines here.

Here’s the full list of the withdrawn CPAP, BiPAP and ventilator machines by Philips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

<<<THE NEW AIRSENSE 11 IS HERE>>>

CHECK IF YOUR CPAP MACHINE HAS BEEN RECALLED