Philips Respironics Dreamstation Recall 2021 (June) Read >> The article gives a detailed description of the best solution for sleep apnea with a reason for recalling the device.
Have you heard about the device made by Philips for patients with sleep apnea? If not, then this article has brought something informational for you.
This article is about – Philips Respironics Dreamstation Recall 2021; this product originated in the United States. If you are not aware of this product, don’t worry.
This article has every minute detail regarding the product and upcoming news about this, keep reading to know more-
What Is Philips Respironics Dreamstation?
The Respironics Dream Station is considered as a helpful solution for the patient suffering from sleep apnea. This sleek-shaped machine has advanced features for increasing the effectiveness of therapy and providing comfort.
If you have seen the recent action of Philips, you must be wondering the reason for Philips Respironics Dreamstation Recall 2021. If you want to know about that, stick to the end of the article. It also has Bluetooth, and it is made compatible with the Dream Mapper app, but you need to download that separately.
How does The Respironics Device work?
When it comes to loved ones suffering from something like sleep apnea, this device is the most prescribed sleep therapy solution for your loved ones. Also, because of being the quietest and simplest BiPAP, it doesn’t disturb the sleep of others.
But due to some reported issues from the family members of the patient on the product. The decision of Philips Respironics Dreamstation Recall 2021 is taken.
What Is The Reason For Recalling The Devices?
Recently, Philips has recalled 3-4 million devices after diagnosing the medical device maker of Philips. It is being said that machines or ventilators, including foam, could potentially increase the chances of cancer or health issues to the patients.
The device could emit toxic chemicals and carcinogenic effects. The customer reported finding black debris in the air rube and feeling sick. The defect determined by them is related to the polyester-based polyurethane in the sound abatement foam of the device.
Solution Given In Philips Respironics Dreamstation Recall 2021
The company has shown regrets for the inconvenience and said to replace the sound- abatement foam with another material. The solution Philips came up with is to co-operate with the user sending them a letter to register the affected devices online for replacement or repairing.
Also, for safety measures, Philips advised discontinuation in the use of affected devices, but not without consulting doctors with an alternative. In case if you have not received the suggestive letter from Philips, call on this number – 877-907-7508. If you want to know more about the Respironics device, click here to know
In the final verdict of the article, hope you got every detail regarding the device and reason for Philips Respironics Dreamstation Recall 2021. You are advised to use the device with utmost safety.
The device comes with the manual and new instructions; now, make sure to follow that. Have you ever used this device before? Comment below.
Do you know the reason for recalling? Mention your comment here.