{
  "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": "2026-04-28",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "manufacturer_contact_zip_ext": "",
      "manufacturer_g1_address_2": "",
      "event_location": "",
      "report_to_fda": "",
      "manufacturer_contact_t_name": "",
      "manufacturer_contact_state": "",
      "manufacturer_link_flag": "Y",
      "manufacturer_contact_address_2": "OSTED",
      "manufacturer_g1_city": "",
      "manufacturer_contact_address_1": "AAHOLMVEJ 1-3",
      "manufacturer_contact_pcity": "",
      "event_type": "Injury",
      "report_number": "3003442380-2026-05774",
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      "manufacturer_address_2": "",
      "pma_pmn_number": "K160648",
      "date_of_event": "20260302",
      "reprocessed_and_reused_flag": "N",
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      "exemption_number": "",
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      "reporter_occupation_code": "003",
      "manufacturer_contact_plocal": "",
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      "distributor_zip_code_ext": "",
      "manufacturer_g1_postal_code": "",
      "manufacturer_g1_state": "",
      "reporter_country_code": "US",
      "manufacturer_contact_area_code": "",
      "date_added": "20260331",
      "manufacturer_contact_f_name": "",
      "device_date_of_manufacturer": "20241017",
      "previous_use_code": "U",
      "device": [
        {
          "device_event_key": "",
          "implant_flag": "",
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          "date_removed_year": "",
          "serviced_by_3rd_party_flag": "N",
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          "brand_name": "QUICK SET",
          "generic_name": "UNO QUICK-SET 110/6 SC1 MECA",
          "manufacturer_d_name": "UNOMEDICAL DEVICES S.A. DE C.V.",
          "manufacturer_d_address_1": "AVE. FOMENTO INDUSTRIAL L9 M3",
          "manufacturer_d_address_2": "PARQUE INDUSTRIAL DEL NORTE",
          "manufacturer_d_city": "REYNOSA, TAMAULIPAS, C.P,",
          "manufacturer_d_state": "",
          "manufacturer_d_zip_code": "88736",
          "manufacturer_d_zip_code_ext": "",
          "manufacturer_d_country": "MX",
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          "catalog_number": "",
          "lot_number": "6009683",
          "other_id_number": "",
          "device_availability": "No",
          "device_report_product_code": "FPA",
          "device_age_text": "",
          "device_evaluated_by_manufacturer": "N",
          "combination_product_flag": "N",
          "udi_di": "05705244017931",
          "udi_public": "05705244017931",
          "openfda": {
            "device_name": "Set, Administration, Intravascular",
            "medical_specialty_description": "General Hospital",
            "regulation_number": "880.5440",
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        }
      ],
      "product_problems": [
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        "Loose or Intermittent Connection"
      ],
      "reporter_state_code": "CA",
      "manufacturer_zip_code": "",
      "suppl_dates_mfr_received": "",
      "mfr_report_type": "Thirty-Day",
      "manufacturer_contact_country": "DA",
      "date_changed": "20260401",
      "health_professional": "",
      "summary_report_flag": "N",
      "manufacturer_g1_zip_code_ext": "",
      "manufacturer_contact_extension": "",
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      "manufacturer_contact_phone_number": "",
      "patient": [
        {
          "patient_sequence_number": "1",
          "date_received": "20260331",
          "sequence_number_treatment": [
            ""
          ],
          "sequence_number_outcome": [
            ""
          ],
          "patient_age": "NA",
          "patient_sex": "Unknown",
          "patient_weight": "",
          "patient_ethnicity": "",
          "patient_race": "",
          "patient_problems": [
            "No Clinical Signs, Symptoms or Conditions"
          ]
        }
      ],
      "distributor_city": "",
      "date_report": "20260303",
      "initial_report_to_fda": "",
      "distributor_state": "",
      "event_key": "",
      "manufacturer_g1_country": "",
      "manufacturer_contact_city": "LEJRE,",
      "mdr_report_key": "24737921",
      "removal_correction_number": "",
      "number_devices_in_event": "",
      "date_manufacturer_received": "20260303",
      "manufacturer_name": "",
      "report_source_code": "Manufacturer report",
      "remedial_action": [
        ""
      ],
      "manufacturer_g1_zip_code": "",
      "report_to_manufacturer": "",
      "manufacturer_zip_code_ext": "",
      "manufacturer_g1_name": "",
      "adverse_event_flag": "N",
      "distributor_address_1": "",
      "manufacturer_state": "",
      "distributor_address_2": "",
      "manufacturer_postal_code": "",
      "single_use_flag": "Y",
      "manufacturer_country": "",
      "mdr_text": [
        {
          "mdr_text_key": "397146428",
          "text_type_code": "Description of Event or Problem",
          "patient_sequence_number": "0",
          "text": "REFERENCE NUMBER (B)(4). EVENT OCCURRED IN CHINA. IT WAS REPORTED THAT THE PATIENT EXPERIENCED INFUSION SET LEAKAGE EVENT ON (B)(6) 2026. THE LEAKAGE WAS AT THE QUICK RELEASE AS THE PATIENT WAS NOT ABLE TO CONNECT IT TIGHTLY. NO FURTHER INFORMATION AVAILABLE."
        }
      ],
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      "distributor_name": "",
      "manufacturer_g1_address_1": "",
      "distributor_zip_code": "",
      "manufacturer_contact_postal_code": "4320",
      "manufacturer_contact_exchange": "",
      "manufacturer_contact_pcountry": "",
      "suppl_dates_fda_received": ""
    }
  ]
}