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  2. A $1 billion CPAP recall devastated Philips. The CEO’s ...

    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 ...

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

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    It was the latest blow to Philips over the recall of millions of sleep apnea and respiratory devices, which has been ongoing since 2021. ... shared to date are adequate to fully evaluate the risks ...

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

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

    AMSTERDAM (Reuters) -Philips shares surged 35% early on Monday as the medical devices maker announced a smaller-than-expected settlement to resolve claims over recalled breathing devices in the ...

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

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    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 ...

  6. Philips settles one category of U.S. claims over respirator ...

    www.aol.com/news/dutch-company-philips-reaches-u...

    AMSTERDAM (Reuters) -Philips said on Thursday it has reached a settlement to resolve one category of legal claims against it following a major recall of the Dutch medical equipment maker's sleep ...

  7. FDA warning letter - Wikipedia

    en.wikipedia.org/wiki/FDA_Warning_Letter

    It is important that third parties reading Warning Letters understand that matters that FDA Warning Letters describe may have been subject to subsequent interaction between the FDA and the recipient that may have changed the regulatory status of the issues discussed. [6] (See the "External links" section below for electronic access to Warning ...

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

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    Philips was recalling some models of the Panorama 1.0T HFO device in the U.S. due to risk of explosion during a "quench procedure" caused by excessive buildup of helium gas. During the procedure ...