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  "documentTitle": "iRhythm Technologies, Inc. (IRTC)",
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      "text": "The FDA Found That iRhythm Products and Practices Put Patients' Lives At Risk",
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      "text": "Despite iRhythm frequently touting its products as the \"gold standard\", the Zio AT contained several fatal flaws. As revealed in an FDA Form 483... the Zio AT had been designed with a transmission limit... which prevented the device from meeting the definition of an MCT.",
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      "text": "iRhythm's products are relatively low-technology devices... all medical-grade cardiac monitors use the same electrode measurement techniques... cardiologists rarely rely on supplier final reports and almost always read the raw strip data to form their own diagnosis.",
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      "text": "Similar to the Zio XT, the device is returned to iRhythm after the wear period for final analysis of patient data. The Zio AT was heralded by the Company as a disruptive product that would incrementally increase iRhythm's addressable market.",
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