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