If you’re a patient in the United States and you’ve registered your device for remediation, this site will allow you to check the status of your replacement device order. If you are a non-U.S. patient, please contact your homecare provider for updates.On this site, you can: Check ...
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 m...
Philips recall toll-free number: 877-907-7508. Latest update: On 8/2/2022, Philips has been asked by the FDA (Federal drug administration) to set your replacement CPAP for your recalled device with your pressure settings BEFORE shipping to you directly. Only your Durable Medical Equipment ...
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...
Three years later, the recallremains ongoingand has prompted investigations by theFood and Drug Administrationand theJustice Department. On Jan. 25, the embattled manufacturer announced it woulddiscontinue the saleof all of its breathing devices in the U.S. In short, a medical device that promised...
Those who return a recalled Philips machine by the August deadline are entitled to both the return and payment awards without having to submit a claim form and can use prepaidshipping labels by clicking hereat no cost. Those who spent their own money buying a comparable replacement CPAP or ve...
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...
Outside of the US, we will continue sales and support of our current sleep and respiratory products. Importantly for patients, these changes to our portfolio do not affect our commitment to the remediation of devices included in theJune 2021 recallof certain CPAP, BiPAP, and mecha...
Those who spent their own money buying a comparable replacement CPAP or ventilator to replace a recalled device will need to complete a device replacement claim form, which can be found here. A paper device replacement form can also be found here or by calling 1-855-912-3432. ...
When he heard about the recall, Callendar did what he says the company told him to do and sent it back for a refund, replacement or repair. "They said they would expedite it," he said, but, "It took them over two years. Two years with my conditions, and it's absolutely unforgivable...