Philips Respironics announced a voluntary recall for Continuous and Non-Continuous Ventilators (certain CPAP, BiLevel PAP and Ventilator Devices) due to two issues related to the polyester-based polyurethane (PE-PUR) sound abatement foam used in these devices. For information on the Recall Notice, a complete list of impacted products, and potential health risks, visit https://philips.com/src-update
Philips has established a registration process that allows Patients, Users, or
Caregivers to look up their device serial number and begin a claim if their unit is affected. To register your device and begin a claim. visit https://www.philipssrcupdate.expertinquiry.com Dismiss
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