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Recall on some Philips CPAP or BiPAP Respironics Positive Airway Pressure devices used for sleep apnea 

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Just got this email from the VA.

Recall on some Philips CPAP or BiPAP Respironics Positive Airway Pressure devices used for sleep apnea 

Your safety is our top priority. VA has learned of the recall on some Philips Respironics Positive Airway Pressure devices (CPAP or BiPAP) used for sleep apnea. If you do not have a Philips Respironics device, it is not part of the recall and you can ignore this email.

Why did they recall this device?

Philips Respironics recently recalled some CPAP and BiPAP devices because very small foam particles may break loose and travel through the air hose during use. This breakdown may also release small amounts of chemical vapors. At this time no serious adverse health events have been reported but Philips has received reports of headache, upper airway irritation, cough, chest pressure and sinus infection.  

Per Philips Respironics, this foam breakdown is more likely in devices that are more than three years old, are used in high heat and humidity environments (more than 95 degrees) or that were cleaned with an ozone or ultraviolet sterilizer.

What should I do if I use this device?

If you use a Philips Respironics CPAP or BiPAP device, such as a Dream Station or System 1, continue to use your device as prescribed and:

  • As soon as possible, register your device on the Philips Respironics website or call 877-907-7508. Philips Respironics will send you a new device when one is available and provide a box for you to return your old device. Devices are replaced based on when they are registered, and replacement may take up to a year.
  • If you and your care provider decide you can safely pause use of your device until a new one is available, this will not impact your VA disability compensation benefits.
  • Only clean your device according to the manufacturer’s instructions.

Do not attempt to remove the sound reduction foam yourself. This can’t be done without breaking the device.

Our records indicate that you are not registered with the VA for your health care. If you are concerned about using your current device, call your regular care provider to schedule an appointment and discuss your options.

For more information on the recall, visit the Philips Respironics Recall website or the Veterans Affairs Philips Respironics Recall site for Frequently Asked Questions.

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