Phillips is recalling millions of sleep apnea machines and ventilators as they pose a serious health risk and they have advised consumers to stop using them immediately. A foam piece used in devices can degrade and release potentially toxic fumes into the patients. Some of the devices and ventilators being recalled are used for treating coronavirus patients.
The exposure to foam particles could cause headache, irritation, inflammation, respiratory issues, and possible toxic and carcinogenic effects, Philips said. The company will replace the current sound abatement foam with a new material and has already begun the preparations, which include obtaining the relevant regulatory clearances. Philips aims to address all affected devices in scope of this correction as expeditiously as possible.
The devices being recalled are Bi-Level PAP, CPAP and mechanical ventilator devices which are primarily first-generation DreamStation products.
For more information on the recall and devices covered and affected by the recall please click on the link below at www.philips.com/SRC-update.
If you or a loved one has suffered from a lung issue and/or lung cancer caused by a Phillips CPAP Machine and/or Ventilator, please call the experts at Inserra Kelley Sewell to see whether you might be entitled to compensation.
6 Comments
Jessica Simpson
Y husband has this machine and is experiencing breathing problems.
Margaret McDonnell
Are there a model number or something were we can check to see if we are using the recall devices?
Jared Israel
The Philips page on this is at
https://www.usa.philips.com/healthcare/e/sleep/communications/src-update?fbclid=IwAR2-KOaOlLD-GdjuGpT-Zgfa88zKYjAg3LFPweTKpvcK5P1Dolt89ZerR1I
Good luck!
Tonya Hibbert
Husband uses this cpap machine
Mary Ruth Wind
My machine quit working about 6 weeks ago. Have not been sleeping well before it quit. I am using old c pap machine from a long time ago.
Low Buen Chek
I bought my Philip CPAP in 2018. I develop lung cancer in 2019
Comments for this article are closed.