Philips CPAP Lawsuit Update
Millions of recalled Philips DreamStation, CPAP, BiPAP and ventilator machines may release toxic foam particles and chemicals into the air pathway.
Millions of recalled Philips DreamStation, CPAP, BiPAP and ventilator machines may release toxic foam particles and chemicals into the air pathway.
A ProPublica report reveals that Philips officials hid thousands of reports of problems with sound abatement foam used in millions of CPAP machines, failing to recall the devices for more…
Philips is asking a federal judge to delay considering motions to remove some CPAP recall lawsuits to state court until the parties get a better idea of how many plaintiffs…
A $479 million Philips CPAP class action settlement agreement will resolve claims of economic loss filed by users of the recalled devices.
The FDA has classified a Carina ventilator PE-PUR foam warning as a class I recall, indicating the breathing devices could put children in particular at an increased risk of cancer…
The FDA warns that 73,000 recalled Trilogy Evo ventilators manufactured by Philips Respironics may be prone to airway blockage from dust and dirt, which has led to at least one…
The Dräger ventilator recall came after tests revealed PE-PUR sound insulation foam was releasing a toxic gas which could cause life-threatening health problems, including cancer.
Philips faces increasing legal concerns in Europe over its recalled Philips DreamStation CPAP devices, which have been linked to deaths there as well as in the U.S.
The FDA has announced a class I recall of nearly 60,000 Philips ventilators, which may not detect air flow blockages due to the build-up of debris.