On June 14, 2021, Philips Respironics* issued a voluntary recall on specific brands of their continuous positive airway pressure (CPAP) machines, bi-level positive airway pressure (BiPAP) machines, and ventilators. Philips Respironics has established a registration process that allows patients, users or caregivers to look up their device’s serial number and initiate a claim if their unit is affected.

 

Use the following link to view the recall information and register your device: usa.philips.com/healthcare/e/sleep/communications/src-update.

 

Members may also call Philips Respironics at 877-907-7508 with questions. We highly recommend that devices be registered to appropriately identify all recalled units and so that impacted patients, users and caregivers receive the most up to date information from Philips Respironics.

 

* Phillips Respironics is an independent company providing medical devices on behalf of Anthem Blue Cross and Blue Shield.

ALLCARE-0979-21

630-0621-EM-NE



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Voluntary recall of Philips Respironics CPAP machine, BiPAP machine, and ventilators