Recalled Philips CPAP Machines Linked to Nearly 400 Deaths By FDA Medical Device Reports
The FDA has announced it has received 106,000 medical device reports linked to recalled Philips CPAP devices, including nearly 400 deaths.
The FDA has announced it has received 106,000 medical device reports linked to recalled Philips CPAP devices, including nearly 400 deaths.
Lawyers are working to register and file Philips CPAP lawsuits, as the manufacturer may argue the June 14 anniversary of a massive recall triggered the start of the statute of…
Philips has set aside about $630 million to resolve potentially thousands of CPAP recall lawsuits filed in courts nationwide.
Philips is posting deceptive numbers on its website representing how many replacement or repaired CPAP machines it has shipped to consumers, the FDA warns.
THe FDA has given a recall of nearly 1,100 reworked Philips DreamStation breathing devices a class I designation, following dozens of reports of the devices malfunctioning or failing to deliver…
Philips CEO Roy Jakobs says the company hopes to reach CPAP settlement agreements on economic loss lawsuits this year, and personal injury lawsuits in 2024.
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.