FDA Addresses Philips CPAP Recall Concerns and Provides Answers to Frequently Asked Questions
The FDA has released a list of Frequently Asked Questions for those affected by the recall of millions of Philips CPAP machines.
The FDA has released a list of Frequently Asked Questions for those affected by the recall of millions of Philips CPAP machines.
Philips has agreed that all DreamStation CPAP lawsuits filed in federal courts should be consolidated before one judge for pretrial proceedings.
A DreamStation CPAP and BiPAP machine class action lawsuit calls for the manufacturer to refund and replace machines recalled because they contain toxic foam which could release particles and gases…
The FDA warns some 200,000 devices included in a recent Philips CPAP recall, including BiPAP machines and mechanical ventilators, may place patients at a greater risk, due to their role…
A quarterly earnings report reveals Philips warned investors about problems with millions of CPAP and similar breathing machines weeks before it warned consumers their health might be in danger.
Two class action lawsuits seek to force Philips to reimburse those with recalled DreamStation CPAP machines for the cost of replacing the devices, which contain sound abatement foam that can…
The JPML has been asked to consolidate all Philips DreamStation CPAP recall lawsuits before one judge for pretrial proceedings.
A class action lawsuit calls for Philips to refund and replace recalled DreamStation CPAP machines, and to provide medical monitoring for users who may have inhaled or ingested cancer-causing, toxic…
The FDA is urging consumers affected by the Philips CPAP and BiPAP recall to heed warnings about the risks of respiratory injuries linked to degrading sound abatement foam.
A recent Philips DreamStation CPAP recall is raising questions as to what role third party cleaning devices using ozone or ultraviolet radiation may have played in customer illnesses.