{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-09-08",
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      "manufacturer_contact_city": "AUDUBON",
      "mdr_report_key": "18677518",
      "removal_correction_number": "",
      "number_devices_in_event": "",
      "date_manufacturer_received": "20200729",
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      "remedial_action": [
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      "mdr_text": [
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          "mdr_text_key": "335024055",
          "text_type_code": "Description of Event or Problem",
          "patient_sequence_number": "0",
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        },
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          "text": "INVESTIGATION CONFIRMED THAT THERE WAS NO SYSTEM MALFUNCTION FOUND. THE ROOT CAUSE WAS USER TECHNIQUE. THIS ISSUE DOES NOT POSE A RISK TO HEALTH AND THERE ARE NO NEW SAFETY CONCERNS ASSOCIATED WITH THIS ISSUE."
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}