Recall Notification Philips Respironics Sleep and Respiratory Care devices
Philips recently issued a product recall for specific ventilators and sleep apnea devices.
Immediate Actions to be taken by You, the User:
1. Discontinue use of your device and work with your physician or Durable Medical Equipment (DME) provider to determine the most appropriate options for continued treatment. To continue use of your device due to lack of alternatives, consult with your physician to determine benefit of continuing therapy with your device.
2. Register your device on the recall website:
a. The website provides you current information on the status of the recall and how to receive permanent corrective action to address the issues.
b. The website also provides you instructions on how to locate your device Serial Number and will guide you through the registration process.
c. Call 877-907-7508 if you cannot visit website.