Phillips Respironics Medical Device Recall Notification
Veterans Health Administration sent this bulletin at 07/15/2021 01:27 PM EDT|
Wilmington VA Medical Center Update |
Wilmington VA
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News & Announcements |
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Phillips Respironics Medical Device Recall Notification Your safety is our top priority. VA has learned of the recall of 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. Philips Respironics recently recalled some CPAP and BiPAP devices due to a breakdown of the foam used to reduce sound and vibration. While in use, recalled devices may have very small foam particles break loose and travel through the air hose. This breakdown may be related to exposure to extreme heat and humidity or the use of unapproved cleaning devices. Therefore, do not use ozone or ultraviolet light-based cleaners per the Food and Drug Administration recommendations.
VA requests that you register your device through the Philips Respironics patient portal at:
Philips Respironics will send a replacement device. This may take several months. Reporting respiratory symptoms Reporting device problems Clinical questions
Other medical device questions
Otherwise, you should continue to use your device as prescribed and clean it using the manufacturer’s instructions. We are currently working with the manufacturer on a solution and will keep you informed as additional information and guidance becomes available. More information Stay Informed, Follow Our Social Media Channels Follow Wilmington VA Medical Center on our social media channels @WilmingtonVAMC on Facebook, Twitter and Instagram. |


