FDA: Philips Respironics Must Fix or Refund Recalled Sleep Devices - Consumer Notice

Modes of mechanical ventilation

Food and Drug Administration

Medical equipment

Philips

Respironics

Continuous positive airway pressure

Medical device

Federal Food, Drug, and Cosmetic Act

Non-invasive ventilation

Sleep apnea

FDA Center for Devices and Radiological Health

Gerald McGinnis

FDA: Philips Respironics Must Fix or Refund Recalled Sleep Devices - Consumer Notice. View article details on HISWAI: https://www.consumernotice.org/news/fda-philips-respironics-must-fix-or-refund-recalled-sleep-devices/