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Severe injuries from recalled Phillips® brand CPAP & BIPAP devices
Victims that suffered serious medical conditions due to recalled Phillips® brand CPAP & BIPAP devices should get a free, private case evaluation.
- Cancer
- Respiratory inflammation and
- Other toxic effects
Phillips® has announced that the company is recalling between 3 and 4 million CPAP and ventilation devices due to disintegrating sound-reducing foam.
Consumers have begun to report severe side effects, including kidney/liver damage, wide-ranging chemical poisonings, and other unhealthy conditions.
Many consumers experience severe and long-lasting side effects from the chemical from the recalled machines, including cancers, strokes, and a variety of cancers.
Consumers that have used particular Phillips® CPAP and ventilation machines and suffered any of these symptoms should come forward to file claims for compensation — legal case evaluations are free of charge and private.
With a surge in the number of Philips© CPAP ventilators and machines linked to respiratory issues, chemical poisonings, and much more, recalls on this medical equipment are also more frequent.
Important Update
The FDA just dropped an update on that Philips sleep apnea machine recall, and it's quite an eye-opener. They're saying these machines might be connected to a whopping 561 reported deaths.
Since April 2021, the FDA has been flooded with over 116,000 reports about these respiratory devices. They've been breaking down and causing some serious health risks. This includes talking, choking, inhaling weird particles, and even an increased chance of cancer.
These devices, used for sleep apnea and similar disorders, were made with a foam called polyester-based polyurethane (PE-PUR). However, this foam breaks down over time, and the little bits can end up in the airways of the people using them. The FDA warns you might end up breathing in these "black pieces of foam" or some invisible chemicals.
After the first recall of over 5 million devices in 2021, Philips tried to sort out the issue. But they still fail to meet safety standards or consumer expectations.
Philips has now agreed to stop selling these devices in the U.S., primarily because of the filing of a proposed class action settlement.
About 80% of the affected devices are CPAP machines and about 20% are ventilators, Philips® spokesman Steve Klink told Reuters.
Most of the devices come from Philips’ DreamStation® line—more than half of the affected devices are in the U.S., according to Philips®.
The recall affects all serial numbers of the following affected devices manufactured between 2009 and April 26, 2021.
In January 2022, the FDA announced that Trilogy Evo® ventilators and Trilogy Evo® repair kits not originally recalled in the July 2021 recall were added to the identified devices list.
Those who qualify may request a free, private case evaluation by a personal injury attorney!
Find Out if You Qualify
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Phillips® has announced that the company is recalling between 3 and 4 million CPAP and ventilation devices due to disintegrating sound-reducing foam.
Consumers have begun to report severe side effects, including kidney/liver damage, wide-ranging chemical poisonings, and other unhealthy conditions.
Many consumers experience severe and long-lasting side effects from the chemical from the recalled machines, including cancers, strokes, and a variety of cancers.
Consumers that have used particular Phillips® CPAP and ventilation machines and suffered any of these symptoms should come forward to file claims for compensation — legal case evaluations are free of charge and private.
With a surge in the number of Philips© CPAP ventilators and machines linked to respiratory issues, chemical poisonings, and much more, recalls on this medical equipment are also more frequent.
About 80% of the affected devices are CPAP machines and about 20% are ventilators, Philips® spokesman Steve Klink told Reuters.
Most of the devices come from Philips’ DreamStation® line—more than half of the affected devices are in the U.S., according to Philips®.
The recall affects all serial numbers of the following affected devices manufactured between 2009 and April 26, 2021.
In January 2022, the FDA announced that Trilogy Evo® ventilators and Trilogy Evo® repair kits not originally recalled in the July 2021 recall were added to the identified devices list.
Those who qualify may request a free, private case evaluation by a personal injury attorney!
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Victims that suffered severe injuries and medical conditions due to recalled Phillips® brand CPAP & BIPAP devices should receive justice and compensation for losses.
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