The FDA is again warning that recalled Philips Trilogy ventilators which were reconditioned and sent back to customers as fixed, may still contain residue of toxic sound abatement foam and…
A new report by Philips claims it found little health risk to consumers from recalled CPAP devices that were not exposed to ozone cleaning methods like those used by SoClean…
The CPAP brain cancer lawsuit says the combination of Philips CPAP sound abatement foam and SoClean's ozone emissions released toxic particles to be inhaled by users.
A Philips DreamStation lawsuit claims toxic sound abatement foam used in the recalled sleep apnea machine led to the development of adenocarcinoma of the lung.
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…
