05 Nov CPAP Machine Recalls: What Should Users Do?
In June 2021, Philips, a maker of many CPAP machine models, announced a voluntary recall of millions of their products. The company reported that the foam used in the machines might deteriorate, resulting in the potential inhalation of toxic particles. This could cause injury or death, and researchers associate dangerous particles with cancer as well as other health issues. The recall is a frightening development for those who depend on these devices to maintain their health.
Millions of patients with sleep apnea or other breathing disorders now need to find a safe alternative for their CPAP or BiPAP machine. These Phillips’ clients cannot afford to ignore the recall, but many are unsure of how to proceed.
Affected CPAP Machines
Not all Philips’ products are affected. The recalled CPAP machines are mostly first-generation DreamStation models. The DreamStation 2 models do not have the same problem and are considered safe to use. Still, the recall affects between 3 and 4 million devices worldwide – all distributed between July 2009 and April 2021. Philips sold half of these defective models in the United States, so American users need to be especially vigilant. Anyone using a CPAP machine needs to determine whether it’s included in the recall. The potential danger from the affected machines should be taken seriously.
Recalled CPAP Machine Effects
The FDA has received over 1200 complaints since Philips issued the recalls. Users have also reported more than 100 injuries related to the deteriorating foam. Industry insiders expect that number to grow.
Consumers have reported black debris inside the machine’s tubing that they were unknowingly ingesting and/or inhaling. A significant portion of these machine owners have also reported headaches, inflammation, respiratory issues, vomiting, and other health problems potentially related to the foam.
Of course, experts do not yet know the long-term effects of this toxic foam, but the scope of the recall indicates the company has serious worries about its consumers’ health.
Recalled CPAP Next Steps
If Philips recalled your CPAP or BiPAP model, you should discontinue its use immediately and consult with your medical professional for advice on the next steps. Simply stopping the use of your model without a replacement machine or treatment can put your health in danger. If your life-sustaining ventilator was affected, do not stop using it before consulting your physician.
Philips has listed the recalled devices and steps to take here. The company also announced they’re working to resolve this issue, providing updated use instructions and a repair and replacement program for the defective machines. In addition, Philips sent out letters to all users with program registration instructions. The company advises those who did not receive a letter to call 877-907-7508 for more information. Many consumers have not yet received the help they need.
CPAP Alternatives
Even before this CPAP recall, many patients were unhappy with their sleep disorder treatment. Like them, you may have found that sleeping while hooked up to a machine is inconvenient, uncomfortable, and less effective than you hoped. Some patients benefit from surgery, but most choose this invasive method as a last resort. Fortunately, viable alternatives to these treatments do exist.
Everyone deserves a goodnight’s sleep and should be able to get it without the use of a machine, medication, or surgery.
Content found on this blog is intended for educational purposes only and should not be used as a substitute for professional judgement, advice, diagnosis, or treatment. Please speak with a professional if you have concerns about your oral or sleep health.