Sleep Apnea Patients with Recalled Philips CPAP Machines Still Waiting for Replacements: Report
An estimated 2.2 million consumers have not received replacements for their recalled Philips CPAP machines
An estimated 2.2 million consumers have not received replacements for their recalled Philips CPAP machines
Volatile organic compounds found in the recalled Philips BiPAP machines can enter users' airways, putting them at risk of serious injury or death, according to an FDA update that categorized the problems as a Class I recall.
Lawsuit alleges Philips DreamStation CPAP machine carried no warnings of possible cancer risks from exposure to deteriorating sound abatement foam inside the device
Court approved registry will help create a census of Philips CPAP claims being investigated by lawyers, and toll the statute of limitations before lawsuits are filed.
The settlement by Philips Respironics resolves allegations raised in a whistleblower lawsuit brought by an employee.
Lawsuit claims foam particles from Philips CPAP machine caused pulmonary fibrosis, emphysema and other symptoms of lung damage.
The recalled Philips CPAP masks have magnets which that may cause problems for heart devices and other medical implants, the FDA warns
Another Philips BiPAP machine recall has been announced over toxic plastic materials that may release cancer-causing volatile organic compounds (VOC) into user's airways.
Eight years after buying and usuing a Philips RemStar CPAP device, the plaintiff was diagnosed with lung cancer and elevated liver enzymes.
Philips CPAP machine PE-PUR foam has been linked to more than 69,000 incidents of cancer, pneumonia, asthma, chest pain, death and other health complications.