Philips Respironics has issued a recall for certain PAP devices including DreamStation PAP devices manufactured before April 26, 2021. The newer DreamStation 2 is not affected.
The recall relates to the type of foam used to reduce the noise made by the devices. Over time, the foam inside the machine may degrade into particles. These particles can enter the humidifier, tubing and mask and patients may inhale the particles when using the device. Philips reports that the potential risks include headache, skin or eye irritation and asthma. Philips also found that the foam can produce unsafe chemical levels. These “volatile organic compounds” are released as gases and may cause problems including irritation of the airway, headache or dizziness, skin, eye or nose irritation, and nausea or vomiting.
Patients can find more information about the recall here: Philips Recall Information. This link allows patients to register and then look up their device to see if it is affected by the recall. If their device is affected, the link allows patients to request assistance. Patients can contact Philips Respironics directly through the link or by telephone at (877) 907-7508 for additional information and assistance with their PAP devices related to the recall.
Philips has issued this advice to patients:
For patients using life-sustaining mechanical ventilator devices:
- Do not stop or alter your prescribed therapy until you have talked to your physician. Philips recognizes that alternate ventilator options for therapy may not exist or may be severely limited for patients who require a ventilator for life-sustaining therapy, or in cases where therapy disruption is unacceptable. In these situations, and at the discretion of the treating clinical team, the benefit of continued usage of these ventilator devices may outweigh the risks.
- If your physician determines that you must continue using this device, use an inline bacterial filter. Consult your Instructions for Use for guidance on installation.
- 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.
The American Academy of Sleep Medicine has guidance for patients here: American Academy of Sleep Medicine Guidance for Patients. There is additional information for clinicians here: American Academy of Sleep Medicine Clinical Guidance. Key information includes:
“Philips advises that patients using recalled BPAP and CPAP devices should stop using their devices and consult with their medical providers to determine the most appropriate options for continued treatment, based on the benefits of continuing therapy and potential identified risks. The AASM suggests that the medical provider prescribe for their patient a PAP device that is not affected by the recall. However, in the case that this is not an option, or another device is unavailable, then it is the AASM viewpoint that clinical factors such as comorbidities, severity of symptoms, risks associated with PAP discontinuation, and safety-sensitive roles should inform the decision to continue or discontinue therapy. This decision should be made in concert between the patient and their medical provider. The ultimate judgment regarding any specific care must be made by the treating clinician and the patient, taking into consideration the individual circumstances of the patient, available treatment options, and resources. The AASM advises that patients contact their medical provider as soon as possible to discuss whether to continue or discontinue treatment.”
Devices affected by the recall include the popular DreamStation CPAP, Auto CPAP and BiPAP units. The newer DreamStation 2 is not affected.
If you use a Philips device, please contact Philips at Philips Recall Information or (877) 907-7508. If you are an Advanced Sleep Medicine Services patient and need additional assistance after contacting Philips, please contact us at customerservice@sleepdr.com or (877) 775-3377.
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Posted on October 10, 2023Thank you for sharing this crucial information. It’s important for people to be aware of the recall on certain Philips Respironics PAP devices. The potential risks outlined highlight the significance of addressing the issue promptly. Stay informed, and if you or someone you know uses these devices, make sure to follow the recall guidelines provided by Philips to ensure safety. Your health matters, and being proactive in response to such notices is a vital step.
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Posted on October 16, 2023I hope that not many people are disadvantaged by this outcome. They should be given new products
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Posted on October 16, 2023It’s essential to be aware of these issues, especially if you use one of the affected devices manufactured before this date.
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Posted on October 17, 2023I really appreciate you because you give very informative content to the users.
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Posted on October 18, 2023Thank you for this amazing content that help readers like me.
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Posted on October 20, 2023This article so give me information that i need thanks for admin.
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Posted on October 21, 2023Valuable Post. appreciated. Keep Posting posts like this about these kind of Devices
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Posted on October 24, 2023Nice Article!
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Posted on October 26, 2023Nice Article
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Posted on October 26, 2023Thanks to your immediate action to recall this certain pap devices. All the best!
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Posted on October 29, 2023Excellent Information, truly problem solved.
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Posted on November 07, 2023Thanks for acting right away to recall these pap machines. Best of luck!
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Posted on November 08, 2023Nice Article!
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Posted on November 11, 2023Thank you so much for this post. Now I can sleep peacefully. i will recommend this to my friends
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Posted on November 16, 2023Thank you so much for writing this. Now I can sleep soundly. I’ll tell my friends about it.
Md Shakil
Posted on November 22, 2023Dear Philips Respironics,
I would like to commend you for taking prompt action and issuing a recall for certain PAP devices, specifically the DreamStation PAP devices manufactured before April 26, 2021. It is commendable that you prioritize the safety and well-being of your customers.
Your clear and detailed communication regarding the recall is highly appreciated. Providing patients with specific instructions on how to check if their device is affected and offering assistance through registration and direct contact channels demonstrates your commitment to ensuring their peace of mind.
The guidance you have provided to patients using life-sustaining mechanical ventilator devices is particularly important. Acknowledging the critical nature of these devices and advising patients to consult with their physicians first shows a deep understanding of their unique circumstances. Suggesting the use of inline bacterial filters as an additional precautionary measure is a valuable piece of advice.
Similarly, your advice to patients using BiLevel PAP and CPAP devices to discontinue usage and work closely with their physicians or Durable Medical Equipment (DME) providers is crucial for maintaining their health and safety. By providing links to the American Academy of Sleep Medicine’s guidance for patients and clinical professionals, you have shown your commitment to supporting patients in making informed decisions.
Overall, your proactive response to this issue and the consideration you have shown toward the well-being of your customers are highly commendable. Thank you for prioritizing safety and providing comprehensive support during this recall.
Sincerely,
Md Shakil
Cameron Johnson
Posted on November 24, 2023I am very concerned about this recall, as I have been using a DreamStation PAP device for several years to treat my sleep apnea. I have not noticed any symptoms of foam degradation or chemical exposure, but I am worried about the potential long-term effects on my health. I have contacted Philips through the link provided and registered my device, but I have not received any response or assistance from them yet. I have also consulted with my physician, who advised me to continue using the device with an inline bacterial filter until I can get a replacement. I hope Philips will act quickly and responsibly to resolve this issue and provide safe and effective PAP devices for their customers.
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Posted on November 27, 2023Today I read many articles but your article is very good and indepth about this sleep disease insomenia. Really its a Nice Article!
I recently started having problem insomenia so i was quite worried. But this article really solved my problem.
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Posted on December 12, 2023Good Job….Valuable and problem-solving content.
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Posted on December 19, 2023I’m delighted you brought up the drawbacks of utilizing a PAP machine. For patients who want to raise awareness, this is a must-share piece of content!
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Posted on December 19, 2023Indeed PAP device is not for everyone. Thanks for such a detailed article.
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Posted on December 26, 2023Thank you so much for writing this. Now I can sleep soundly. I’ll tell my friends about it.
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Posted on December 26, 2023Thank you so much for this detailed article on the recall of certain Philips PAP Devices. My Doctor had given me minimal information on the recall – this helped to answer more of my questions! Appreciated the info!
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Posted on January 08, 2024Thank you for the update on the recall of certain Philips PAP devices. Please provide more details or guidance on next steps for affected users. Appreciate your prompt communication on this matter.
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Posted on January 17, 2024This article so give me information that i need thanks for admin.
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Posted on January 17, 2024Thank you for sharing this informative article. The details about the Philips Respironics recall are crucial for user safety, and this information has been very enlightening for me.
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Posted on January 18, 2024It’s crucial to check the recall status using the provided link and take necessary steps for assistance if affected. Patient safety is a top priority.
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Posted on January 30, 2024I had a product like this and it was making a lot of noise. I wonder if I should return it back.
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Posted on January 31, 2024Great Piece of information
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Posted on February 11, 2024I must say that you are an inspiration to other. Thanks very much.
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Posted on February 15, 2024It’s concerning to hear about the recall for certain Philips PAP devices.
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Posted on February 18, 2024Your words of appreciation truly inspire and motivate me. Thank you very much for your kind acknowledgment.
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Posted on February 20, 2024hi there very helpfull blog
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Posted on February 21, 2024Thanks I was suffering from Insomnia from long days this article really helped me so much.
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Posted on February 25, 2024This decision should be made in concert between the patient and their medical provider.
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Posted on March 01, 2024It’s always recommended to follow the recall guidelines provided by Philips for our safety.
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Posted on March 03, 2024All of such devices are really useful in different use purpose. But its better to use them in right way.
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Posted on March 07, 2024Wow, I had no idea about the potential dangers lurking in Philips devices due to foam degradation. It’s scary to think about inhaling particles and exposure to unsafe chemicals while using these products. I’m glad Philips is taking action, but this raises concerns about product safety. Thanks for sharing this important information!
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Posted on March 24, 2024We have to be very careful in order to stay up to date with the latest trends and recalls for our devices
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Posted on April 17, 2024Thank you so much for writing this. Now I can sleep soundly. I’ll tell my friends about it.
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Posted on April 26, 2024If your physician determines that you must continue using this device, use an inline bacterial filter.
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