Sleep Labs to Autoscoring Software Developers: Prove It
Survey data shows sleep lab leaders prioritize validation and certification when implementing sleep study autoscoring software.
Survey data shows sleep lab leaders prioritize validation and certification when implementing sleep study autoscoring software.
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.
Until the requirements of the consent decree are met, Philips Respironics will not sell new CPAP, BiPAP, or other respiratory care devices in the US.
Gerald “Jerry” E. McGinnis, founder of Respironics, died on Jan 25 at age 89.
Read MoreCongressional investigators are launching an inquiry into the FDA’s oversight of medical device recalls following reports that the agency failed to issue warnings about breathing machines capable of sending hazardous particles and fumes into the lungs of patients.
Read MoreMedical providers and patients who leased, rented, or purchased recalled Philips CPAPs, BiPAPs, or ventilators—as well as payers who reimbursed recalled devices—can now file a claim for a share in the company’s $479 million settlement deal.
Read MorePhilips Respironics has paid $2,471,359.25 to resolve allegations that it violated the False Claims Act by giving kickbacks to sleep laboratories, according to the U.S. Attorney’s Office for the Southern District of California.
Read More“With Every Breath,” a new documentary from ProPublica and the Pittsburgh Post-Gazette, is an intimate glimpse into what happens when patients and a doctor learn that a lifesaving device may be causing harm.
Read MoreFollowing warnings that CPAP masks with magnetic closures may interfere with certain medical devices and implants, sleep physicians have questions. Here’s what to know.
Read MorePhilips raised its 2023 earnings outlook following an uptick in third-quarter sales, despite ongoing challenges related to its CPAP and ventilator device recall.
Read MoreUS Senator Dick Durbin and US Representative Jan Schakowsky have introduced legislation to reform medical device recalls in an effort to improve patient safety.
Read MoreSen. Richard Blumenthal is calling for “immediate, aggressive action” against Philips for keeping known defects with the company’s CPAP machines secret.
Read MorePhilips Respironics says it plans to conduct additional testing on certain CPAP and respiratory devices involved in its June 2021 recall at the request of the FDA.
Read MoreProPublica and the Pittsburgh Post-Gazette have filed suit against the US Food and Drug Administration, accusing the agency of holding back records related to the recall of breathing machines.
Read MoreA look at answers to some of the most critical questions about the ongoing recall of millions of CPAP machines, ventilators, and other breathing devices.
Read MorePhilips is responding to recent media articles that claim the company knew about safety issues with certain CPAP machines and ventilators for years before recalling the devices in June 2021.
Read MoreTo understand the breakdowns that led to one of the most tumultuous medical device recalls in generations, ProPublica and the Pittsburgh Post-Gazette spent a year probing what happened inside Philips Respironics after the company first learned that contaminants were turning up in breathing machines designed to save lives.
Read MorePhilips knew about a dangerous breakdown inside its widely used CPAP machines and ventilators but waited years before recalling the devices, according to an investigation by ProPublica and the Pittsburgh Post-Gazette.
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