Overview
The litigation lawyers at Smith, Gildea & Schmidt, LLC are looking into the Philips CPAP recall. In June of 2021, Philips issued an Urgent Medical Device Recall for many of its CPAP and BiPAP machines. These machines are most-often used to treat sleep apnea. Philips admits in the urgent recall that its machines can cause serious, life-threatening and permanent injuries including asthma and cancer. Other injuries also include headache, trouble breathing, cough, chest discomfort, and sinus infection.
Have You Been Affected by the CPAP Recall?
CPAP Related Injuries Include:
- Cancer
- Asthma
- Kidney Disease
- Liver Disease
- Skin, Eye, Lung, and Throat Irritation
- Headaches
- Dizziness
- Nausea
- Vomiting
Check Your CPAP Machine Serial Number
If you would like to know whether your machine is part of Philips’ CPAP Recall, click here to visit a website that will allow you to look up the serial number of your CPAP machine. If you need assistance locating your serial number, please click here for a guide to show you where the serial number is located on your Philips CPAP machine.
Recalled CPAP Machines Include:
- Trilogy 100
- Trilogy 200
- Garbin Plus, Aeris, LifeVent
- A-Series BiPAP Hybrid A30 (not marketed in US)
- A-Series BiPAP V30 Auto
- A-Series BiPAP A40
- A-Series BiPAP A30
- E30 (Emergency Use Authorization)
- DreamStation ASV
- DreamStation ST, AVAPS
- SystemOne ASV4
- C-Series ASV
- C-Series S/T and AVAPS
- OmniLab Advanced+
- SystemOne (Q-Series)
- DreamStation
- DreamStation Go
- Dorma 400
- Dorma 500
- REMstar SE Auto
Our CPAP Recall litigation lawyers represent clients on a contingency fee basis, meaning there is no legal fee unless you receive compensation.
