We use cookies to provide you with a better experience. By continuing to browse the site you are agreeing to our use of cookies in accordance with our Cookie Policy.
Accept
Home » Philips Concludes Recalled Sleep Therapy Devices Not Likely to Cause Harm
Philips Concludes Recalled Sleep Therapy Devices Not Likely to Cause Harm
Philips Respironics reports risk assessments of its continuous positive airway pressure (CPAP) and bi-level positive airway pressure (BiPAP) sleep apnea therapy devices showed that degraded sound abatement foam on the devices would likely not cause “appreciable harm” to patient health.