Once again, the US Food and Drug Administration is alerting patients and health care providers about potential risks with some sleep apnea treatment devices from Royal Philips. In a 29 August safety communication, the FDA says certain Philips Respironics bi-level positive airway pressure (BiPAP) machines may contain a plastic contaminated with non-compatible material.
If that plastic is in the device motor, the FDA says it may release volatile organic compounds (VOCs), which are...
Read the full article – start your free trial today!
Join thousands of industry professionals who rely on Medtech Insight for daily insights
- Start your 7-day free trial
- Explore trusted news, analysis, and insights
- Access comprehensive global coverage
- Enjoy instant access – no credit card required
Already a subscriber?