If you’re among the millions of people who rely on Philips CPAP machines for a good night’s sleep, you may be concerned about the recent recall of certain models due to potential health risks. In this article, we’ll provide you with information about the recall, including how to find the original video announcement from the FDA and what to do if your CPAP machine is affected. We’ll also discuss the potential health risks associated with the recalled machines and provide tips for staying safe while using a CPAP machine. For more information and the latest updates, be sure to visit the Bonshop website.
I. How To Find Original Video Of Recalled Philips Cpap Machines
Search YouTube For Official FDA Announcement
One simple way to find the original video of the FDA announcement is to search for it on YouTube. While there may be many videos that discuss or cover the recall, the official FDA announcement will likely be among the top search results.
Check The FDA Website
Another way to find the original video is to visit the FDA website. The FDA has a section dedicated to the recall of Philips CPAP machines, where you can find various resources, including the official announcement video.
Philips Respironics Website
Philips Respironics, the manufacturer of the recalled CPAP machines, also has a section on their website dedicated to the recall. There, you can find the official video announcement from the FDA, as well as other important information and resources related to the recall.
Contact Philips Respironics Customer Service
If you are unable to find the original video announcement using the above methods, you can contact Philips Respironics customer service for assistance. They may be able to provide you with a link to the video or other information about the recall.
II. What is the Official Announcement From FDA
FDA Recall Notice
The FDA issued a recall notice on June 14, 2021, for certain Philips CPAP, BiPAP, and mechanical ventilator devices due to potential health risks associated with the foam used in the devices.
The FDA stated that the foam may degrade over time and release toxic chemicals, which can cause serious health problems, including cancer and respiratory issues.
- Philips DreamStation CPAP and BiPAP machines
- Philips E30 CPAP and BiPAP machines
- Philips OmniVent mechanical ventilator
- Philips A-Series BiPAP V30 ventilator
- Philips C-Series ASV ventilator
The FDA recommends that patients stop using the recalled devices and contact their healthcare provider to discuss alternative treatment options.
III. What to Do if Your CPAP Machine Has Been Recalled
Contact Your Doctor
If you are using a Philips CPAP machine that has been recalled, you should contact your doctor as soon as possible. Your doctor can help you determine if you are at risk for any health problems and can recommend the best course of action.
Stop Using Your CPAP Machine
You should immediately stop using your Philips CPAP machine if it has been recalled. Using a recalled CPAP machine can put you at risk for serious health problems, including cancer and respiratory failure.
|Potential Health Risks
|Unusual lumps or growths, unexplained weight loss, fatigue, skin changes
|Severe shortness of breath, rapid heart rate, confusion, bluish tint to the skin or lips
Return Your CPAP Machine
Once you have stopped using your CPAP machine, you should return it to Philips Respironics. Philips Respironics has issued a voluntary recall of all affected CPAP machines. You can find more information about the recall and how to return your machine on the Philips Respironics website.
Get a New CPAP Machine
If you need a new CPAP machine, you should talk to your doctor about your options. There are a variety of CPAP machines available, and your doctor can help you find one that is right for you.
It is important to note that the recall was issued due to a potential health risk related to the foam in certain CPAP, BiPAP, and Mechanical Ventilator devices. Philips Respironics has issued a voluntary Field Safety Notice (outside U.S.) / voluntary recall notification (U.S. only) and has remediated 99% of actionable sleep therapy device registrations to date. If you or someone you know has been affected by this recall, please visit the Philips Respironics website for more information.
The information in this article comes from various sources, including Wikipedia and newspapers. We’ve tried to make sure it’s accurate, but we can’t guarantee that every detail is 100% correct. So, be careful when using this article as a source for your research or reports.