Philips CPAP Recall
If you've suffered negative health affects due to a defective Philips CPAP, BiLevel PAP, or Ventilator device we can help. Contact us today to discuss your claim.
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Philips has recently recalled 4 million CPAP (continuous positive airway pressure), BiLevel PAP (bi-level positive airway pressure), and similar devices containing sound abatement foam liners made from polyester-based polyurethane (PE-PUR).
This foam can degrade into particles that users can then inhale or ingest and also emit carcinogenic toxic gas chemicals. The devices contain no filter to prevent this inhalation or ingestion of volatile organic compounds including Diethylene glycol, Toluene Diisocyanate, Toluene Diamine, and Phenol Dimethyl Diazine.
Furthermore, high heat or humidity can cause PE-PUR to degrade further. Some users have even reported seeing black debris in their breathing tubes – evidence of foam degradation. These recalled devices are defective products that are unreasonably dangerous, and can potentially lead to serious health conditions including cancer.
If you are using one of the recalled Philips sleep apnea devices, you should consulting with a healthcare provider, preserve your machine for evidence, and contact an attorney as soon as possible to discuss your claim.
Call 212-268-3222 or contact us online to speak with an experienced product liability lawyer at Raphaelson & Levine Law Firm today.
The recalled Philips products include Bi-Level Positive Airway Pressure (Bi-Level PAP), Continuous Positive Airway Pressure (CPAP) and mechanical ventilator devices manufactured before April 26, 2021.
The recall is related to PE-PUR foam that can degrade into particles which may be inhaled, or produce certain chemical emissions.
The recalls applies to specific, but not all models of Philips' CPAP devices. The recall does not apply to CPAP machines made by other manufacturers.
Philips voluntarily recalled four million of the following CPAP , BiLevel PAP , and mechanical ventilator devices, including approximately 300,000 devices which were distributed to veterans through the VA:
Continuous Ventilator, Minimum Ventilatory Support, Facility Use
Continuous Ventilator, Non-life Supporting
Non-continuous Ventilator
Continuous Ventilator
Continuous Ventilator, Minimum Ventilatory Support, Facility Use
Continuous Ventilator, Non-life Supporting
If you are using a Philips CPAP device, to check if your device is one of those being recalled find the model and serial number of your device on a sticker affixed to the machine by looking at its bar code or simply typing in the information here: https://www.usa.philips.com/c-w/support-home/find-model-number.html
Philips Apnea devices which were meant to improve people’s breathing are in fact contaminating people's airways. These defective devices listed above were recalled because they have design flaws that make them unreasonably dangerous, and can potentially result in cancer, pulmonary fibrosis, lung injury, and other serious long-term health issues.
According to a recent Philips press release:
These issues can result in serious injury which can be life-threatening, cause permanent impairment, and/or require medical intervention to preclude permanent impairment.
Users of these CPAP devices has also reported symptoms including chest pressure, sore throats, and sinus infections.
Victims of the recalled sleep apnea devices may be eligible to recover compensation for medical expenses, lost wages, loss of future earning, and pain and suffering. In cases that go to trial, you may also be awarded punitive damages if the court finds Phillips acted in a malicious or a gross negligent manner — such as if Philips knew about the hazards and risks and took no action to fix the issue.
If you or a loved one have been injured by a defective Philips CPAP machine, the experienced product liability lawyers at Raphaelson & Levine can help. Our attorneys have recovered more than $700 Million on behalf of clients throughout New York.
Call 212-236-3222 or contact us online to schedule a free consultation today.
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