A product liability lawsuit claims sound abatement foam used in a Philips Respironics DreamStation Auto CPAP device cause a man to develop lung cancer.
A fatal case of lung cancer was caused by exposure to sound abatement foam in recalled Philips CPAP devices, a deceased woman's husband claims.
The FDA is proposing an order to force Philips Respironics to submit a plan to replace, repair or refund consumers who are stuck with millions of CPAP sleep apnea machines…
A Maine woman says she had to undergo a double-lung transplant due to exposure to toxic sound abatement foam used in Philips CPAP devices.
Philips has announced it has received a subpoena from the Justice Department regarding its problematic Philips CPAP machine recalls, indicating a federal investigation may be underway.
A product liability lawsuit claims exposure to toxic sound abatement foam used in Philips' DreamStation sleep apnea machines resulted in pancreatic cancer.
A tolling agreement reached in February has led to a significant drop in the number of Philips CPAP lawsuits being filed in federal courts nationwide.
A medical supplier is seeking class action status for a lawsuit claiming Philips misled them into selling defective products to their customers which put them in danger of serious illness.
A Dreamstation CPAP lawsuit claims exposure to toxic sound abatement foam led a man to suffer acute respiratory failure.
The FDA has released instructions for consumers on how to have the replacement of their recalled Philips CPAP device prioritized.