06/17/2021
UPDATE: This week Philips Respironics announced a voluntary national manufacturer's recall for some of its Continuous and Non-Continuous Ventilators (certain CPAP, BiLevel PAP and Ventilator Devices) due to two issues related to the polyester-based polyurethane (PE-PUR) sound abatement foam used in these devices.
For information on the Recall Notice, a complete list of impacted products, and potential health risks, visit philips.com/src-update.
If you have an affected product, you must contact Philips Respironics directly at philips.com/src-update to register your device for repair / replacement and to keep updated on the latest information about this manufacturer’s recall. Scroll down to the "Patients, Users, and Caregivers" section and look for the link starting on 6/17/21.
RSM patients using affected devices may contact our office for further treatment recommendations. We ask for your patience as we return your calls since this manufacturer’s recall has affected millions of patients and their devices across the nation. RSM is committed to do our best to assist our patients during this time.
Please remember, that if you have an affected device, you must contact Respironics directly for repair/replacement of your device. We also recommend that you check back with their site frequently for updates on the recall as this evolves.
Thank you!
