{
  "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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    {
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      "report_to_fda": "N",
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      "manufacturer_contact_address_2": "",
      "manufacturer_g1_city": "",
      "manufacturer_contact_address_1": "",
      "manufacturer_contact_pcity": "",
      "event_type": "Injury",
      "report_number": "MW5005534",
      "type_of_report": [
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      ],
      "product_problem_flag": "N",
      "date_received": "20080212",
      "manufacturer_address_2": "",
      "pma_pmn_number": "",
      "date_of_event": "20080128",
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      "reporter_occupation_code": "RISK MANAGER",
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      "manufacturer_g1_postal_code": "",
      "manufacturer_g1_state": "",
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      "manufacturer_contact_area_code": "",
      "date_added": "20080225",
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      "device": [
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          "date_removed_flag": "",
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          "date_received": "20080212",
          "brand_name": "SLIP-CATH BEACON TIP CATHETER",
          "generic_name": "SLIP-CATH",
          "manufacturer_d_name": "COOK INC.",
          "manufacturer_d_address_1": "750 DANIELS WAY",
          "manufacturer_d_address_2": "",
          "manufacturer_d_city": "BLOOMINGTON",
          "manufacturer_d_state": "IN",
          "manufacturer_d_zip_code": "47404",
          "manufacturer_d_zip_code_ext": "",
          "manufacturer_d_country": "US",
          "manufacturer_d_postal_code": "47404",
          "device_operator": "HEALTH PROFESSIONAL",
          "expiration_date_of_device": "20110131",
          "model_number": "G11993",
          "catalog_number": "*",
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          "device_evaluated_by_manufacturer": "",
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          "udi_di": "",
          "udi_public": "",
          "openfda": {
            "device_name": "Catheter, Intravascular, Diagnostic",
            "medical_specialty_description": "Cardiovascular",
            "regulation_number": "870.1200",
            "device_class": "2"
          }
        }
      ],
      "product_problems": [
        "Migration or Expulsion of Device",
        "Other (for use when an appropriate device code cannot be identified)",
        "Device, removal of (non-implant)"
      ],
      "reporter_state_code": "TX",
      "manufacturer_zip_code": "",
      "suppl_dates_mfr_received": "",
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      "manufacturer_contact_country": "",
      "date_changed": "20250813",
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      "summary_report_flag": "N",
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      "manufacturer_contact_extension": "",
      "manufacturer_city": "",
      "manufacturer_contact_phone_number": "",
      "patient": [
        {
          "patient_sequence_number": "1",
          "date_received": "20080212",
          "sequence_number_treatment": [
            ""
          ],
          "sequence_number_outcome": [
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          ],
          "patient_age": "86 YR",
          "patient_sex": "",
          "patient_weight": "101",
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          "patient_problems": [
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            "Foreign body, removal of",
            "Surgical procedure, additional"
          ]
        }
      ],
      "distributor_city": "",
      "date_report": "20080212",
      "initial_report_to_fda": "",
      "distributor_state": "",
      "event_key": "",
      "manufacturer_g1_country": "",
      "manufacturer_contact_city": "",
      "mdr_report_key": "1000009",
      "removal_correction_number": "",
      "number_devices_in_event": "",
      "manufacturer_name": "",
      "report_source_code": "Voluntary report",
      "remedial_action": [
        ""
      ],
      "manufacturer_g1_zip_code": "",
      "report_to_manufacturer": "",
      "manufacturer_zip_code_ext": "",
      "manufacturer_g1_name": "",
      "adverse_event_flag": "Y",
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      "manufacturer_state": "",
      "distributor_address_2": "",
      "manufacturer_postal_code": "",
      "single_use_flag": "",
      "manufacturer_country": "",
      "mdr_text": [
        {
          "mdr_text_key": "788212",
          "text_type_code": "Description of Event or Problem",
          "patient_sequence_number": "1",
          "text": "PROCEDURE: IVC FILTER PLACEMENT. THE SLIP-CATH BEACON TIP CATHETER INADVERTENTLY PASSED THROUGH THE INTERNAL JUGULAR INTO THE RIGHT SUBCLAVIAN ARTERY. PT HAD A HIGH INR WHICH INCREASED THE PT'S POTENTIAL FOR BLEEDING UPON REMOVAL OF THE SLIP-CATH BEACON TIP CATHETER. THEREFORE, FOR THE SAFETY OF THE PT, THE PT WAS TAKEN TO THE OR FOR REMOVAL OF THE SLIP-CATH BEACON TIP CATHETER AND SUTURING OF THE SUBCLAVIAN ARTERY. DATES OF USE: 2008. DIAGNOSIS OR REASON FOR USE: PLACEMENT OF IVC FILTER."
        }
      ],
      "number_patients_in_event": "",
      "distributor_name": "",
      "manufacturer_g1_address_1": "",
      "distributor_zip_code": "",
      "manufacturer_contact_postal_code": "",
      "manufacturer_contact_exchange": "",
      "manufacturer_contact_pcountry": "",
      "suppl_dates_fda_received": ""
    }
  ]
}