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  1. 2 lut 2024 · Philips has agreed to stop selling sleep apnea machines in the U.S. and existing devices manufactured between 2009 and April 2021 are subject to recall, as they may pose a serious injury...

  2. 29 sty 2024 · Based on the latest test results for the CPAP/BiPAP sleep therapy devices, is Philips Respironics saying they are safe for patients to use? The extensive data and results now available for the first-generation DreamStation, System One

  3. 21 sie 2022 · Philips said last week it is about halfway through replacing the 5.5 million devices, which include mechanical ventilators as well as non-invasive breathing devices used to treat sleep apnea,...

  4. 4 lut 2024 · The Food and Drug Administration says 561 deaths have been reported in connection to recalled Philips devices to treat obstructive sleep apnea and other breathing disorders.

  5. The issue relates to certain ventilators, Philips CPAP (Continuous Positive Airway Pressure) and BiPap (Bi-Level Positive Airway Pressure) sleep apnea devices. The affected products are identified in the tables below:

  6. 29 kwi 2024 · Millions of CPAP sleep apnea machines made by the medical device maker Philips and a subsidiary were found to have a dangerous problem, triggering consumer lawsuits and a massive recall...

  7. In June 2021, after discovering a potential health risk related to the foam in certain CPAP, BiPAP and Mechanical Ventilator devices, Philips Respironics issued a voluntary Field Safety Notice (outside U.S.) / voluntary recall notification (U.S. only).

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