{
  "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_contact_zip_ext": "",
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      "manufacturer_contact_plocal": "",
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          "manufacturer_d_address_1": "3651 BIRCHWOOD DRIVE",
          "manufacturer_d_address_2": "",
          "manufacturer_d_city": "WAUKEGAN",
          "manufacturer_d_state": "IL",
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          "device_availability": "Yes",
          "device_report_product_code": "KGO",
          "device_age_text": "",
          "device_evaluated_by_manufacturer": "",
          "combination_product_flag": "N",
          "udi_di": "",
          "udi_public": "",
          "openfda": {
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      ],
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      "mfr_report_type": "",
      "manufacturer_contact_country": "",
      "date_changed": "20250807",
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      "summary_report_flag": "N",
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      "manufacturer_contact_extension": "",
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      "patient": [
        {
          "patient_sequence_number": "1",
          "date_received": "20200609",
          "sequence_number_treatment": [
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          ],
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            "No Known Impact Or Consequence To Patient"
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      ],
      "distributor_city": "",
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      "distributor_state": "",
      "event_key": "",
      "manufacturer_g1_country": "",
      "date_report_to_manufacturer": "20200609",
      "manufacturer_contact_city": "",
      "mdr_report_key": "10133418",
      "removal_correction_number": "",
      "number_devices_in_event": "",
      "date_report_to_fda": "20200511",
      "manufacturer_name": "",
      "report_source_code": "User Facility report",
      "remedial_action": [
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      "manufacturer_g1_zip_code": "",
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      "adverse_event_flag": "N",
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      "manufacturer_state": "",
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      "single_use_flag": "",
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      "mdr_text": [
        {
          "mdr_text_key": "194495514",
          "text_type_code": "Description of Event or Problem",
          "patient_sequence_number": "1",
          "text": "STERILE GLOVES WERE SEEN TO HAVE MICRO TEARS. OTHER GLOVES (X3) FROM THE SAME LOT WERE CHECKED BUT WERE OK."
        }
      ],
      "number_patients_in_event": "",
      "distributor_name": "",
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      "manufacturer_contact_exchange": "",
      "manufacturer_contact_pcountry": "",
      "suppl_dates_fda_received": ""
    }
  ]
}