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

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

    Philips sent a letter to all its affected customers in December, requesting them not to position a patient's lower limbs directly under the detector. These devices were manufactured and ...

  3. Monitoring (medicine) - Wikipedia

    en.wikipedia.org/wiki/Monitoring_(medicine)

    A medical monitor or physiological monitor is a medical device used for monitoring. It can consist of one or more sensors, processing components, display devices (which are sometimes in themselves called "monitors"), as well as communication links for displaying or recording the results elsewhere through a monitoring network.

  4. Mayo Clinic Florida - Wikipedia

    en.wikipedia.org/wiki/Mayo_Clinic_Florida

    Impressed by the medical treatment received by members of Jacksonville's Davis family (then owners of the Winn-Dixie supermarket chain) at Mayo Clinic in Minnesota, they rallied community and corporate support to bring Mayo Clinic to Jacksonville and donated a 392-acre parcel off San Pablo Road on which Mayo Clinic opened an outpatient consultation center on October 6, 1986.

  5. 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 ...

  6. Mayo Clinic Hospital (Rochester) - Wikipedia

    en.wikipedia.org/wiki/Mayo_Clinic_Hospital...

    Additionally, Mayo was the only hospital on the 2016–2017 honor roll to also receive 5 stars from CMS. [21] Every Mayo Clinic hospital received an "A" safety rating from Leapfrog in its April 2017 report. [22] In 2019–20, Mayo Clinic, Rochester, was ranked again as the #1 overall hospital in the United States by U.S. News & World Report.

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

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

    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.

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