{
  "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": "2026-08-05",
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          "manufacturer_d_address_1": "1100 CAMPUS ROAD",
          "manufacturer_d_address_2": "",
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          "manufacturer_d_state": "NJ",
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          "device_report_product_code": "JXG",
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          "combination_product_flag": "N",
          "udi_di": "",
          "udi_public": "",
          "openfda": {
            "device_name": "Shunt, Central Nervous System And Components",
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        "Material Deformation"
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      "suppl_dates_mfr_received": "",
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      "manufacturer_contact_country": "",
      "date_changed": "20250801",
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      "summary_report_flag": "N",
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      "manufacturer_contact_extension": "",
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          "sequence_number_treatment": [
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          "sequence_number_outcome": [
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            "Device Embedded In Tissue or Plaque"
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      ],
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      "distributor_state": "",
      "event_key": "",
      "manufacturer_g1_country": "",
      "date_report_to_manufacturer": "20200427",
      "manufacturer_contact_city": "",
      "mdr_report_key": "10000359",
      "removal_correction_number": "",
      "number_devices_in_event": "",
      "date_report_to_fda": "20200421",
      "manufacturer_name": "",
      "report_source_code": "User Facility report",
      "remedial_action": [
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      "manufacturer_postal_code": "",
      "single_use_flag": "",
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      "mdr_text": [
        {
          "mdr_text_key": "189003052",
          "text_type_code": "Description of Event or Problem",
          "patient_sequence_number": "1",
          "text": "DURING LUMBAR CATHETER INSERTION, THE CATHETER KINKED AND COULD NOT BE ADVANCED. A SECTION OF THE CATHETER LUMBAR CATHETER SECTION BROKE WHILE TRYING TO REMOVE KINKED CATHETER LEAVING A RETAINED FRAGMENT IN SPINAL CANAL. PHYSICIAN DETERMINE THAT THE RETAINED SECTION OF CATHETER WOULD NOT POSE A PATIENT SAFETY ISSUE AND A NEW CATHETER WAS SUCCESSFULLY INSERTED AND PLACED."
        }
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      "distributor_zip_code": "",
      "manufacturer_contact_postal_code": "",
      "manufacturer_contact_exchange": "",
      "manufacturer_contact_pcountry": "",
      "suppl_dates_fda_received": ""
    }
  ]
}