CPAP MACHINES

CPAP and Bi-Level PAP (BiPAP) machines help many people with sleep apnea and other conditions. However, the very machines that many people need in order to breathe may also be releasing dangerous particles and toxins that the user may inhale or ingest during use.

Philips, a manufacturer of CPAPs, Bi-PAP machines and other mechanical ventilator devices recently issued a recall of numerous CPAP and Bi-PAP machines due to potential health risks from potential degradation of sound abatement foam, which is used in these devices to reduce sound and vibration. The foam, which is made of a polyester-based polyurethane (PE-PUR), can break down and potentially enter the device’s air pathway. When this occurs, chemicals and debris can be released and inhaled or swallowed by the person using the device.  This can cause serious injury and permanent impairment, including the development of lung cancer, head, neck and respiratory carcinomas, breathing impairments, pulmonary hypertension, and other chronic respiratory illnesses.

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Recalled devices include:

  • Dreamstation (1st Generation Product Family)

  • C-Series

  • Dorma 400

  • Dorma500

  • REMStar SE Auto

  • SystemOne

  • OmniLab Advanced Plus

Medical devices can provide treatment for serious conditions and provide relief to many people. However, when medical devices have design defects or manufacturing defects, they may cause harm. Our attorneys are experienced in holding manufacturers and distributors accountable for harm caused by design defects, manufacturing defects, and failures to warn.

If you or a loved one have used one of the recalled machines and suffered harm, call our products liability attorneys to schedule a free case review. You can discuss your potential claim with us at no cost by calling us today at 757-223-4545 or by filling out our contact form.