Philips CPAP Recall

 

CPAP machines produced by Philips are recalled due to a potential health risk. Although the recall has not been widespread, the company has received more than 1,200 reports of injuries and complaints. The company will contact registered users to notify them of the issue. For those who have experienced any of these symptoms, a legal action may be possible. Alternatively, they may be entitled to monetary damages if they have sustained organ damage due to their CPAP machine.

The Philips CPAP recall affects a number of their machines. The CPAP DreamStation line is among those affected. This recall is limited to one model, but it affects all serial numbers. The recalled units were manufactured between 2009 and 2021, and more than half of the affected devices are currently on the market in the U.S. The CPAP recalled by Philips includes the DreamStation 2 model, which is not affected by the recall. The degraded foam in CPAP devices is a known cause of health risks, and the manufacturer has a comprehensive repair program available for the recalled CPAP machines. Chemical exposure and toxic effects are some of the most common and serious risks associated with CPAP usage.

The recall affects the DreamStation line of CPAP machines. It affects all serial numbers of recalled CPAP devices. This recall is also applicable to Trilogy Evo ventilators and repair kits, and affected devices are listed on the company's website. Those affected can check if their devices are recalled by contacting the company or the manufacturer for more information. Affected patients may contact the company's manufacturer for more information.

The Philips CPAP recall affects a number of different models, including the DreamStation line. The recall includes all models from 2009 to 2021. This means that more than 50% of CPAP machines in the U.S. are affected. The company has also added Trilogy Evo ventilators and repair kits to its CPAP recall list in January 2022. If you own a Philips CPAP, contact the company for more information on the recalled machines.

The Philips CPAP recall involves two types of ventilation devices. The first model contains a degraded foam. The degraded foam may contain toxic gases and other contaminants. The older the unit is, the more likely it is that it is affected by this issue. A patient who is affected by this CPAP recall may wish to file a lawsuit against the manufacturer. A family member may wish to take legal action on behalf of a loved one.

The Philips CPAP recall affects the DreamStation line, which is similar to ResMed's DreamStation. However, any of the three brands may be an ideal choice for you, depending on the severity of your sleep apnea. Some of these products are more durable than others. If you're concerned about your health, you may want to consult a physician for a replacement.