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  2. US FDA classifies Philips' recall of imaging machines ... - AOL

    www.aol.com/news/us-fda-classifies-philips...

    Philips' recall of BrightView Imaging Systems, used for single photon emission computed tomography (SPECT) scan, is to correct the faulty component and not a product removal, the health regulator ...

  3. US FDA identifies recall of Philips medical imaging devices ...

    www.aol.com/news/us-fda-identifies-recall...

    Philips stopped producing and selling the product line in 2014, according to the company. The company is also grappling with the fallout of a global recall in 2021 of millions of respirators used ...

  4. Philips shares surge on US recall settlement news - AOL

    www.aol.com/news/philips-pays-1-1-billion...

    Philips said it had agreed to pay $1.1 billion to settle all personal injury claims filed in the U.S., ending uncertainty that had slashed its market value over the past three years.

  5. US FDA says 561 deaths related to Philips machines ... - AOL

    www.aol.com/news/us-fda-says-561-deaths...

    The health regulator added that in 2023, between July and September, it received more than 7,000 medical device reports, including 111 reports of deaths related to the use of these machines.

  6. US FDA still not satisfied with Philips recall; stock falls ...

    www.aol.com/news/us-fda-still-not-satisfied...

    It was the latest blow to Philips over the recall of millions of sleep apnea and respiratory devices, which has been ongoing since 2021. "We do not believe that the testing and analysis Philips ...

  7. A $1 billion CPAP recall devastated Philips. The CEO ... - AOL

    www.aol.com/finance/1-billion-cpap-recall...

    Earlier this year, Dutch medical device maker Royal Philips reached a $1.1 billion deal to settle thousands of claims stemming from a recall in 2021 of millions of its breathing machines like ...

  8. US FDA flags new problem with Philips machines, shares fall - AOL

    www.aol.com/news/us-fda-cautions-philips-sleep...

    Philips shares were down 4.9% at 18.58 euros by 1223 GMT. Analysts from ING said in a note that the DreamStation 2 is the successor of the DreamStation 1 machine which had used the problematic foam.

  9. US FDA identifies recall of Philips' respiratory devices as ...

    www.aol.com/news/us-fda-identifies-recall...

    The Dutch medical devices maker started the process on March 29 and has recalled 73,000 devices in the United Sates. Philips was recalling the ventilators after detecting contaminants such as dust ...