Debbie Cenziper

RT @MikeSallah7: EXCLUSIVE: In wake of massive recall, SEC launches investigation into whether Philips Respironics concealed the dangers in…

RT @MikeSallah7: “I still don’t have my husband. But it sounds like a good amount of money coming out of their pocket, so it makes me feel…

Loved seeing grads from the Medill Investigative Lab at Harvard last night for the Goldsmith Prize for Investigative Reporting. All worked on "With Every Breath," a @propublica @PittsburghPG series named one of six Goldsmith finalists @MedillSchool https://t.co/iMKvT7BNgT

RT @smmills1960: NEW: The revelations in this series of stories on Philips CPAP machines just keep coming. From @propublica and @Pittsburgh…

RT @Steve_Bohnel: I've worked in four newsrooms after graduating from @TempleUniv. This investigation by @MikeSallah7, @michael_korsh, @deb…

With Every Breath: Remarkable student journalists at the Medill Investigative Lab traveled the country last year to interview patients impacted by the Philips recall. @MonicaSager3 @mgfleming12 @mollyfburke @sightsonwheels @susantisarkar and others https://t.co/tdFCWaMCf4

Amid recall crisis, Philips Respironics has agreed to stop selling sleep apnea machines in the United States under an agreement with the government. @propublica and @PittsburghPG has been investigating for more than a year. @MikeSallah7 @michael_korsh https://t.co/SiSy4FyuzC

This short documentary on the Philips CPAP recall by @LizMoughon @ProPublica is stunning. https://t.co/Kz5HDqOLvZ

Congressional Watchdog Will Launch Inquiry Into FDA Oversight of Medical Device Recalls Sens. Dick Durbin and Richard Blumenthal called for the investigation, citing stories about Philips Respironics recall by @propublica @PittsburghPG https://t.co/goJWyEWkux

RT @michael_korsh: IMPACT: In response to @PittsburghPG/@propublica’s reporting in “With Every Breath,” Congressional investigators @USGAO…

RT @propublica: A new short documentary from ProPublica and the Pittsburgh Post-Gazette follows patients and a doctor navigating the fallou…

Records show Philips investigated its DreamStation 2 CPAP two years ago and found water inside the devices could cause "loss of therapy, thermal events, and shock hazards." The company concluded the risk was "acceptable" and "containment" unnecessary. https://t.co/xkX7d7I4uV

"If you had grenades and you’re not sure where they’re going to go off, that’s a problem.” Tests find varying levels of formaldehyde in material used in new CPAPs sent out after the 2021 Philips recall. Exclusive reporting by @propublica @PittsburghPG https://t.co/xkX7d7I4uV

RT @propublica: Watch: "With Every Breath" follows patients and a doctor navigating the fallout of the massive recall of Philips breathing…

https://t.co/De4HWUQCTL

Senator Dick Durbin @SenatorDurbin

An outrage to find @propublica's new report confirms @US_FDA dropped the ball on the Phillips recall. The agency received at least 30 reports about CPAP machines BEFORE Phillips initiated the recall—but did not act. Now millions face health risks from these flawed devices.

The FDA knew seven years before the massive Philips recall of breathing machines that material packed inside ventilators could contaminate the air and travel into the lungs of patients. Here's what happened. @michael_korsh @MikeSallah7 https://t.co/De4HWUQCTL

"Why are we still allowing this to happen?" Under the watch of the FDA, medical device makers held back warnings about breakdowns capable of inflicting serious harm -- more than 200,000 last year alone. "With Every Breath" @MikeSallah7 @michael_korsh https://t.co/De4HWUQCTL