If you have a CPAP (continuous positive airway pressure) machine that you use to treat your sleep apnea, you should check it out closely. Philips recently recalled millions of these devices along with many ventilators because of potential health risks.
Philips Warns About Possible Foam Degradation in CPAP Devices
In its 2021 first quarterly report, Philips noted that it had received user reports and testing indicating possible risks to users related to the sound abatement foam used in certain Philips’ sleep and respiratory care devices. This foam helps eliminate sound and vibration from the devices so they operate more quietly. It seems the foam may degrade under certain circumstances, including:- Using unapproved cleaning methods, such as those involving ozone
- High humidity and temperature
Philips Recalls Millions of Devices with Sound Abatement Foam
Philips then provided an update to that warning on June 14, 2021. In that update, the company announced it was issuing a voluntary recall for specific devices including:- Bi-Level Positive Airway Pressure (Bi-Level CPAP)
- CPAP machine
- Mechanical ventilator devices
- Headache
- Irritation
- Hypersensitivity
- Inflammation
- Nausea/vomiting
- Respiratory issues
- Possible toxic and carcinogenic effects
Consumers Should Check with Their Doctors
Based on an analysis of the potential health risks, Philips has advised consumers as follows:- For those with Bi-Level CPAP and CPAP devices—stop using these immediately and talk to your doctor about other options.
- For those using life-sustaining mechanical ventilator devices—talk to your doctor before making any changes. Alternatives may be limited.