Philips Issues DreamStation CPAP/BiPAP Recall Notification

On June 14, 2021 Philips issued a recall notification for specific Philips bi-level positive airway pressure (bi-level PAP), continuous positive airway pressure (CPAP), and mechanical ventilator devices. The recall is in response to potential health risks related to the sound abatement foam component in these devices.  Full details can be found here: https://aasm.org/philips-dreamstation-cpap-recall-notification/. RESMED MACHINES ARE NOT AFFECTED AND ARE NOT PART OF THE RECALL.

Dr. Shim’s recommendation for patients using the recalled machines is as follows: For patients with mild OSA (an AHI less than 15 on their most recent non-titration sleep study), they may temporarily discontinue CPAP therapy until repaired/replaced CPAP/BiPAP machines are available through the manufacturer.

For patients with moderate to severe OSA (an AHI 15 or more on their most recent non-titration sleep study), we recommend continuing with CPAP therapy, as the risk of stopping outweighs the potential harm from off-gassing based on the best available medical advice.

Please contact our office at 503-990-7187, opt. 1 with any additional questions.  We will update this website as new information regarding repair/replacement is available.

Update:

Great news regarding the Philips Respironics CPAP/BiPAP recall! At long last many patients are beginning to receive their replacement machines. If you receive your new machine and have any questions, please call Philips Respironics at 833-262-1871. Our staff is also always happy to help with any questions or concerns.

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