On June 30, 2021, Philips Respironics issued a voluntary recall of several models of their CPAP, BiPAP, and ventilator machines. This recall affects millions of patients worldwide who rely on Philips Respironics medical devices to support their respiratory health. For CPAP users who’ve used this company’s medical equipment for years, hearing the news of this recall has been both frightening and confusing.
Many sleep apnea patients wonder what they should do with their Philips Respironics equipment and what this recall means for their future health. We’re here to help. In this article, we’ll focus on the Philips Respironics recall and what it means for you. But, first, here’s what you should know.
Understanding the Recall
The three types of devices that Philips Respironics recalled on June 30, 2021, are as follows:
- CPAP machinery
- BiPAP equipment
Philips Respironics recalled various models of these devices specifically due to health concerns connected with the noise-canceling foam used in these machines. The most notable machines recalled for CPAP users were the DreamStation, DreamStation ASV, and DreamStation ST.
The Source of the Recall
Philips Respironics’s official recall site states that its machine’s abatement foam was the source of their health concerns. The abatement foam is a polyester-based polyurethane foam designed to reduce the vibration and noise of Philip Respironics machines. However, recent findings concluded that this foam could enter the airway of CPAP, BiPAP, and ventilator machines.
Studies done by Philips Respironics found that black debris leftover from the abatement foam could mix with other toxic chemicals, and users of these devices could inhale or swallow them. As a result, Philips Respironics recalled all equipment with this abatement foam.
What Does This Mean for Philips Respironics CPAP Users?
So, what does this recall mean for users of Philips Respironics CPAP equipment? First, it’s crucial to check if your CPAP machine is on the official Philips Respironics recall list.
If your equipment information matches the recall models on this list, then stop using this machinery immediately.
If your current equipment is a part of this recall, you must speak with your doctor and review the official FDA list of recommendations to consider how to support your sleep cycle during this recall period safely.
Here are some of the most common recommendations doctors are giving patients of these defective devices.
Register Your Equipment on the Official Recall Website
It’s also crucial that any Philips Respironics CPAP users register their devices for recalls online. When you register your device on the official recall website, you immediately receive communications from Philips Respironics regarding updates, instructions, and any urgent FDA information.
These updates will continue to automatically send information to help you stay informed on the status of these recalled machines.
Invest in New or Backup Devices
Most CPAP users all ask the same question amid this massive recall: what do I do now? For patients who suffer from severe sleep apnea, CPAP therapy is vital to maintain their health and wellness. These patients cannot stop using their CPAP equipment completely.
The FDA recommends that patients with recalled CPAP devices speak with their doctors about finding an alternative CPAP device. Doctors can work individually with patients to recommend the best temporary equipment or alternative CPAP devices for their condition.
In addition, patients should consult with their doctors before purchasing new equipment to review how this change could affect their comfort, health, and insurance coverage. Once patients have more information about the type of replacement machine to look for, they can begin to browse and buy CPAP masks online.
Pro Sleep Tip: Using Travel CPAP Equipment as a Temporary Substitute
Taking advantage of miniature travel CPAP equipment is also beneficial. While this equipment does not include all the same features as a regular CPAP machine, mini travel CPAP devices can help while you discuss more permanent options with your doctor.
Add Additional Sleep Apnea Therapies to Your Routine
During this recall period, your doctor may also recommend increasing some natural forms of sleep apnea therapy.
For example, increasing your daily exercise, quitting smoking, and decreasing alcohol consumption can significantly reduce your sleep apnea symptoms.
While these therapies are not a cure for sleep apnea, they are beneficial for maintaining a healthy sleep cycle during this recall period.
Understandably, this recall has caused a great amount of concern and anxiety regarding the safety of using respiratory equipment. Although this is a large recall, both the FDA and Philips Respironics are working together to evaluate the health concerns of their previous equipment and look at how to make future equipment safer.
If you have concerns regarding your CPAP equipment, consult with your doctor immediately to address these concerns, register your recalled equipment, and pursue alternative sleep therapy options. Taking these steps to ensure that your current equipment is safe for use could prevent major health concerns down the road.
As a reference, we hope our guide to understanding the Philips Respironics recall and what it means for you is beneficial. While this recall’s health and safety concerns are valid, staying calm and working closely with your doctor or DME technician is essential.
How Nationwide Medical Can Help
Need help finding new equipment during this recall? Here at Nationwide Medical, we supply some of the highest quality and safest CPAP masks and machines online.
Whether you’re looking to switch your CPAP equipment or need a substitute machine to support your health, we’ve got you covered. We work closely with our customers to find the best fit for their medical needs. To learn more about our devices, services, and dedicated team, explore our Nationwide Medical website for additional information.
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