Patio Drugs has been notified by Philips Respironics, a manufacturer of CPAP and BIPAP devices, that they have issued a voluntary recall on certain devices due to two related issues with the sound abatement foam used in these devices. Your device may be part of the recall. For information on the Recall Notice, a complete list of impacted products, and the potential health risks, please visit www.philips.com/src-update.
The manufacturer has advised that you contact your physician so he/she can determine the benefits of continuing therapy and potential risks. At this time, we are waiting on further guidance from the manufacturer, and we will post updates to our website.
We appreciate your patience and are here if you have any further questions.
For answer to commonly asked questions, please visit the link below (hosted by Philips Respironics):