Philips CPAP Recall

 

The Philips CPAP recall involves more than twenty different models of sleep apnea machines. The recalled devices contain a design defect that can cause toxic chemical emissions from the degraded foam. The inhalation of these substances can have serious consequences. The Shouse Law Group is filing a CPAP lawsuit against Philips on behalf of victims of the CPAP recall, seeking the largest settlement possible.

As a result of the recall, the Philips DreamStation line is among the most affected. The recall affects all models with serial numbers between 2009 and 2021. According to the FDA, more than half of the recalled Philips CPAP devices are still in use in the U.S. In addition, the Trilogy Evo ventilator and repair kits are included on the recalled list. Users are urged to check for and follow the manufacturer's instructions to prevent the CPAP machine from causing harm to their health.

The Philips CPAP recall only affects certain Philips Respironics devices used to treat obstructive sleep apnea. As of the time of this writing, there have been no reports of death or other complications relating to chemical exposure from the recalled units. However, it is important to note that the recalled Philips CPAP devices may have degraded foam that releases toxic gases or chemicals. Inhaling these gasses can have detrimental health and respiratory effects for people who use them.

The Philips CPAP recall has affected many models of CPAP machines. The most affected is the DreamStation line. The affected devices have all serial numbers between 2009 and 2021. More than half of the recalled devices are sold in the U.S. The FDA added Trilogy Evo ventilators and repair kits to its list in January of 2022. If you have a Philips CPAP machine, contact your manufacturer for more information on the recalled device.

The Philips CPAP recall has affected all types of devices, including some types of CPAP machines. This device may have toxic chemicals in it that may cause serious health problems. Those who are allergic to these materials should avoid the device. Alternatively, they may have to stop using the CPAP. Affected patients should contact their healthcare provider immediately to get a replacement. Regardless of the model, a CPAP machine should work well for most patients.

The Philips CPAP recall has affected more than fifty million devices, affecting more than half of those in the U.S. The CPAP manufacturers are offering a comprehensive repair and replacement program. As soon as possible, users should contact their provider for more information. They may also be offered nasal decongestants or even surgical treatments. You should contact the manufacturer of your CPAP device to receive the replacement.