You can use an alternative CPAP machine that is not on the recall list. You may continue to use your affected device on the condition that your physician has determined that the benefits far outweigh the risks. Please consider using alternative sleep apnea treatments for the time being before ...
We strongly encourage you to subscribe (see above) to our recall mailing list for the latest updates. Do I have to ship the unit to the CPAP seller for recall service, or shipped to Philips directly? I do not want the package to be rerouted and thus delay my therapy. It depends. Som...
The recall involves specific Philips Bi-Level Positive Airway Pressure (Bi-Level PAP), Continuous Positive Airway Pressure (CPAP) and mechanical ventilator devices to address potential health risks related to polyester-based polyurethane sound abatement foam that is in the machines, Philips said in a...
On June 30, 2021, the U.S. Food and Drug Administration issued aSafety Communicationabout Philips’ voluntary recall of some of its BiPAP, CPAP and ventilator devices. Philips is the largest producer of CPAPs in the world, as many as four million machines could be affected. People who can...
When Philips first announced the replacement foam it would use to rework the machines, concerns were raised. That same foam is now the cause of this year’s recall update. Next Steps for Consumers After CPAP Recall Update If you, or someone you love, have been using a Philips Respironics ...
Mask: AirFit™ P30i Nasal Pillow CPAP Mask with Headgear Starter Pack Additional Comments: Min EPAP: 8.2, Max IPAP: 25, PS:4 Top Conrad Posts: 594 Joined: Mon Jul 30, 2012 9:10 am Location: Northern Illinois Re: Phillips / Philips Respironics recent recall notice discussion thread Pos...
Initially recalled two-and-a-half years ago, the Food and Drug Administration has since received 105,000 complaints — including 385 reported deaths — tied to leaking foam in the continuous positive airway pressure (CPAP) machines. Philips attempted to fix some of the more than 5 million recal...
Registration for affected CPAP and BiPAP devices in the US and Canada closed on December 31, 2024. The Patient Portal will remain open for registered US patients until June 30, 2025. Learn More > Sleep and Respiratory Care Patients and Caregivers DMEs and Distributors Clinicians Recall ...
Registration for affected CPAP and BiPAP devices in the US and Canada closed on December 31, 2024. The Patient Portal will remain open for registered US patients until June 30, 2025. Learn More > Sleep and Respiratory Care Patients and Caregivers DMEs and Distributors Clinicians Recall ...
Philips Respironics, a manufacturer of CPAP devices, and the FDA issued a recall for their machines in June 2021, after it was discovered that users were likely to inhale or ingest toxic gasses and particles from a part of the machine designed to limit sound and vibration. Among the possible...