Facing criticism and investigations over its handling of a massive Philips CPAP recall last year, the manufacturer is reportedly in negotiations over a consent decree with the Department of Justice.
The FDA has received reports of 260 deaths linked to toxic sound abatement foam which led to a massive Philips CPAP sleep apnea machine recall
The FDA is warning of problems with recalled Philips Trilogy ventilators due to the new liners potentially blocking airways and traces of toxic PE-PUR sound abatement foam.
The FDA warns that face magnets used in recalled Philips CPAP masks carry a serious risk of injury and death for users.
SoClean has amended a complaint it filed a year ago against Philips, adding new information claiming the medical device manufacturer tried to use SoClean CPAP cleaning devices and their use…
A federal judge has issued an order allowing plaintiffs in Philips CPAP lawsuits to file Short Form Complaints attached to a Master complaint to streamline the filing process, as the…
Millions of consumers with recalled Philips CPAP machines have yet to receive replacement units, according to a new report.
A Philips BiPAP machine recall has been given a class I designation by the FDA, indicating volatile organic compounds emitted from the devices could cause serious injury or death.
A California man's Philips DreamStation lawsuit says exposure to sound abatement foam led to the development of throat cancer.
A federal judge has approved a census registry program for all Philips CPAP recall lawsuits filed in federal courts nationwide.
