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.
The Big Story
Thu. Dec 28, 2023
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.
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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.
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.
We found answers to some of the most critical questions about the ongoing recall of millions of CPAP machines, ventilators and other breathing devices.
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.
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The Human Toll of Philips’ Failure to Disclose Dangerous Defects of Its CPAP Devices

A new short documentary from ProPublica and the Pittsburgh Post- Gazette follows patients and a doctor navigating the fallout of the massive recall of Philips breathing machines.

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