CPAp
cpap
Many American purchased CPAP machines to help with sleep apnea or other serious conditions. In June 2021, Philips recalled CPAP machines which it had manufactured. It was revealed that the sound reducing foam in the machines could degrade and release toxic chemicals that cause cancer and organ damage.
The FDA determined that Philips knew the foam in its machines was harmful and degradable at least as early as 2015.
If you believe your Philips device caused cancer or other illness, you may be entitled to financial compensation.
recalled products
The following is a list of products made between 2009 and 2021 that have been recalled by Philips Respironics
- A-Series BiPAP A30
- A-Series BiPAP A40 (ventilator)
- A-Series BiPAP Hybrid A30
- A-Series BiPAP V30 Auto (ventilator)
- C-Series ASV (ventilator)
- C-Series S/T and AVAPS
- DreamStation
- DreamStation ASV
- DreamStation Go
- DreamStation ST, AVAPS
- Dorma 400
- Dorma 500
- E30
- Garbin Plus, Aeris, LifeVent (ventilator)
- OmniLab Advanced+
- REMstar SE Auto
- SystemOne ASV4
- SystemOne (Q-Series)
- Trilogy 100 (ventilator)
- Trilogy 200 (ventilator)
Get Involved Today
Please provide the following information to determine if you qualify for financial compensation.