voluntary recall
Philips Respironics announced a voluntary recall for certain CPAP, BiLevel PAP and Ventilator Devices due to two issues related to the sound abatement foam used in these devices. To register your device for repair or replacement, please go to philips.com/src-update or call Philips Respironics at 877-907-7508. This website also has information on the Recall Notice and a complete list of impacted products. Please note this recall applies to Philips Respironics devices only. We have received no warnings or communication about issues with Resmed or other manufacturer’s devices.
Please complete this questionnaire for assistance managing the Philips Respironics recall. If you are using an ozone based cleaning system, per Philips Respironics discontinue use of the ozone cleaner immediately and clean your equipment per manufacturer’s instructions.
