Michael D. Sallah
Philips Agrees to Pay $1 Billion to Patients Who Say They Were Injured by Breathing Machines
The proposed settlement will effectively end more than 700 lawsuits filed after the 2021 recall of millions of the company’s widely used sleep apnea devices and ventilators.
FDA Repeatedly Rejected Safety Claims Made by Philips After the CPAP Recall but Waited to Alert the Public, Emails Show
As Philips reassured patients that millions of recalled machines were safe, internal emails show federal regulators privately told the company its testing didn’t account for the impact of long-term harm from tainted devices.
Amid Recall Crisis, Philips Agrees to Stop Selling Sleep Apnea Machines in the United States
The breathing machine manufacturer has faced relentless criticism over its handling of the 2021 recall of millions of devices. Philips must meet the requirements outlined in an agreement with the Justice Department before it can resume sales.
Philips Recalled Breathing Machines in 2021. Chemicals of “Concern” Found in Replacement Machines Raised New Alarm.
Amid a massive recall in 2021, the medical device maker Philips raced to overcome troubling questions about its replacement machines as customers waited for help.
“Unacceptable”: Senators Call on GAO to Probe FDA’s Oversight of Medical Devices, Citing Series on Philips CPAP Recall
Sens. Dick Durbin and Richard Blumenthal sent a letter noting how the agency missed opportunities to protect the public from faulty medical devices, citing reporting by ProPublica and the Pittsburgh Post-Gazette.
Millions of People Used Tainted Breathing Machines. The FDA Failed to Use Its Power to Protect Them.
The FDA’s complaint-tracking system for medical devices allowed Philips to obscure when it knew about dangerous CPAPs. New reporting shows the regulatory lapses extend to many devices and companies.
Top Philips Executive Approved Sale of Defective Breathing Machines by Distributors, Despite Tests Showing Health Risks
Philips argued in court that its U.S. subsidiary should be responsible for damages caused by its CPAP machines and ventilators. Patients’ attorneys say safety decisions were made at the Dutch company’s highest levels.
Senator Calls for DOJ Action Against Philips for Keeping CPAP Machine Complaints Secret
The FDA also said it is “unsatisfied” with the company’s response to the crisis. Share prices dropped in early trading.
What You Need to Know About the Philips Respironics CPAP Recall
We found answers to some of the most critical questions about the ongoing recall of millions of CPAP machines, ventilators and other breathing devices.
We Spent a Year Investigating the Philips CPAP Recall. Here’s How We Did It.
An international team of reporters reviewed thousands of records and interviewed insiders to expose what went wrong in the global corporation.
Help ProPublica and the Pittsburgh Post-Gazette Investigate the Recall of Philips Respironics Breathing Machines
If you’ve reported a death or injury or struggled to get a device replaced, we’d like to hear about your experience with the company.
Philips Kept Complaints About Dangerous Breathing Machines Secret While Company Profits Soared
Tainted CPAP machines and ventilators went to children, the elderly and at least 700,000 veterans despite internal warnings. Company insiders said the devices posed an “unacceptable” risk.
