Philips CPAP Health Issues Continue To Surface Long After DreamStation Recall
Users of recalled Philips CPAP devices are continuing to report illnesses linked to exposure to toxic sound abatement foam.
Users of recalled Philips CPAP devices are continuing to report illnesses linked to exposure to toxic sound abatement foam.
Plaintiffs have responded to a motion by Philips to dismiss CPAP injury lawsuits, calling the company's arguments baseless and against a process the manufacturer has already agreed to follow.
The FDA says nearly 14,000 recalled Trilogy and Garbin Plus ventilators have sound abatement foam problems which could put patients at risk of serious injury or death.
The FDA reports it has received more than 98,000 medical device reports linked to degrading sound abatement foam in Philips CPAP machines, including 346 deaths.
Parties have introduced competing deadlines for Philips CPAP lawsuits which could have a large impact on when bellwether cases go before a jury.
A Philips CPAP device lawsuit claims toxic sound abatement foam led to seven years of oral cancer treatments for a New York man.
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.