October 26, 2022 – Millions of respiratory devices that help people sleep were recalled last 12 months due to a possible hazard, and the issue continues to be not resolved.
The problem is that the froth of pressurized CPAP (Continuous Positive Airway Pressure) machines breaks down over time, potentially leaving sleep apnea victims inhaling small particles and dangerous chemicals, Philips' June 2021 warning said.
The company said on the time it could repair or replace the devices inside a 12 months. But in actual fact, the recall has been expanded to over five million devices worldwide, and the Dutch company says the issue could persist into next 12 months.
CPAP machines work by forcing air through a mask in order that the user's airway stays open while they sleep.
Sleep apnea is a serious sleep problem that happens when your respiratory stops and starts when you sleep. If left untreated, it will probably cause loud snoring, daytime sleepiness, or more serious problems like heart problems or hypertension.
Symptoms include snoring, tiredness throughout the day, restlessness during sleep, dry mouth, sudden awakening gasping for air, and night sweats.
Men are more often affected than women; about 10 to 30 percent of adults are affected. Related Press reported.
According to AP, Philips' tests of the recalled devices went well.
The risks of the froth include headaches, asthma, allergic reactions and carcinogenic effects on internal organs, the Food and Drug Administration.
More than 340 personal injury lawsuits have been consolidated against Philips in federal court, the AP reported.