Philips Issues a Recall Notification* to Mitigate Potential Health Risks Related to the Sound Abatement Foam Component in Certain Sleep and Respiratory Care Devices

Philips Issues a Recall Notification* to Mitigate Potential Health Risks Related to the Sound Abatement Foam Component in Certain Sleep and Respiratory Care Devices | FDA

Issue relates to Philips's BiPAP, CPAP and mechanical ventilator devices . . . do tell if you are among these! Keword: PE-PUR