{
  "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": "2026-07-07",
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          "manufacturer_d_address_1": "301 CATRELL DR",
          "manufacturer_d_address_2": "",
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          "device_evaluated_by_manufacturer": "",
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          "openfda": {
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        "Deformation Due to Compressive Stress"
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      "date_changed": "20250728",
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      "manufacturer_g1_country": "",
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      "manufacturer_contact_city": "",
      "mdr_report_key": "10000305",
      "removal_correction_number": "",
      "number_devices_in_event": "",
      "date_report_to_fda": "20200420",
      "manufacturer_name": "",
      "report_source_code": "User Facility report",
      "remedial_action": [
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      "mdr_text": [
        {
          "mdr_text_key": "189012605",
          "text_type_code": "Description of Event or Problem",
          "patient_sequence_number": "1",
          "text": "CENTURION INTRO-FLEX 8.5F SINGLE LUMEN, LOT# 2020020750, EXP 12/31/2020, ECVC6325. DURING PLACEMENT TO RIGHT INTERNAL JUGULAR (IJ), WHILE TRYING TO REMOVE GUIDEWIRE, GUIDEWIRE WAS KINKED, MAKING REMOVAL DIFFICULT. LINE WAS ABLE TO BE SAVED, PATIENT WAS NOT RE-STUCK. GUIDEWIRE AND PACKING PROVIDED FOR REVIEW. LOCATION: EMERGENCY DEPARTMENT."
        }
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      "manufacturer_contact_pcountry": "",
      "suppl_dates_fda_received": ""
    }
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}