Got an email from a DME provider I have used in the past with a link to the FDA website: Certain Philips Respironics Ventilators, BiPAP, and CPAP Machines Recalled Due to Potential Health Risks: FDA Safety Communication.
For affected CPAP and BiPAP devices, Philips is recommending discontinuing usage of an affected device and consult with your healthcare provider. FDA guidance is a little less clear.
No clear timeline to repair affected devices that I can find, but it appears Philips has not yet gotten FDA clearance on any materials that are needed to replace the affected parts.
For affected CPAP and BiPAP devices, Philips is recommending discontinuing usage of an affected device and consult with your healthcare provider. FDA guidance is a little less clear.
No clear timeline to repair affected devices that I can find, but it appears Philips has not yet gotten FDA clearance on any materials that are needed to replace the affected parts.