{
  "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": "2026-06-30",
    "results": {
      "skip": 0,
      "limit": 1,
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    {
      "manufacturer_contact_zip_ext": "",
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      "event_location": "HOSPITAL",
      "report_to_fda": "Y",
      "manufacturer_contact_t_name": "",
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      "manufacturer_contact_address_1": "",
      "manufacturer_contact_pcity": "",
      "event_type": "Death",
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      "type_of_report": [
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      ],
      "product_problem_flag": "Y",
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      "manufacturer_address_2": "",
      "pma_pmn_number": "",
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      "reprocessed_and_reused_flag": "",
      "manufacturer_address_1": "",
      "report_date": "20130509",
      "exemption_number": "",
      "manufacturer_contact_zip_code": "",
      "reporter_occupation_code": "",
      "manufacturer_contact_plocal": "",
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      "manufacturer_contact_l_name": "",
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      ],
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      "manufacturer_g1_postal_code": "",
      "manufacturer_g1_state": "",
      "reporter_country_code": "US",
      "manufacturer_contact_area_code": "",
      "date_added": "20130518",
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      "device": [
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          "implant_flag": "",
          "date_removed_flag": "",
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          "serviced_by_3rd_party_flag": "",
          "date_received": "20130509",
          "brand_name": "DRAEGER INFINITY DELTA",
          "generic_name": "MONITOR, PHYSIOLOGICAL",
          "manufacturer_d_name": "DRAEGER MEDICAL SYSTEMS, INC.",
          "manufacturer_d_address_1": "3135 QUARRY ROAD",
          "manufacturer_d_address_2": "",
          "manufacturer_d_city": "TELFORD",
          "manufacturer_d_state": "PA",
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          "manufacturer_d_zip_code_ext": "",
          "manufacturer_d_country": "US",
          "manufacturer_d_postal_code": "18969",
          "device_operator": "INVALID DATA",
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          "catalog_number": "*",
          "lot_number": "*",
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          "device_availability": "Yes",
          "device_report_product_code": "MHX",
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          "device_evaluated_by_manufacturer": "",
          "combination_product_flag": "",
          "udi_di": "",
          "udi_public": "",
          "openfda": {
            "device_name": "Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)",
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          }
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      ],
      "reporter_state_code": "OH",
      "manufacturer_zip_code": "",
      "suppl_dates_mfr_received": "",
      "mfr_report_type": "",
      "manufacturer_contact_country": "",
      "date_changed": "20250826",
      "health_professional": "",
      "summary_report_flag": "N",
      "manufacturer_g1_zip_code_ext": "",
      "manufacturer_contact_extension": "",
      "manufacturer_city": "",
      "manufacturer_contact_phone_number": "",
      "patient": [
        {
          "patient_sequence_number": "1",
          "date_received": "20130509",
          "sequence_number_treatment": [
            ""
          ],
          "sequence_number_outcome": [
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          ],
          "patient_age": "57 YR",
          "patient_sex": "",
          "patient_weight": "91",
          "patient_ethnicity": "",
          "patient_race": ""
        }
      ],
      "distributor_city": "",
      "date_report": "20130509",
      "initial_report_to_fda": "",
      "distributor_state": "",
      "event_key": "",
      "manufacturer_g1_country": "",
      "date_report_to_manufacturer": "20130517",
      "manufacturer_contact_city": "",
      "mdr_report_key": "3118744",
      "removal_correction_number": "",
      "number_devices_in_event": "",
      "date_report_to_fda": "20130509",
      "manufacturer_name": "",
      "report_source_code": "User Facility report",
      "remedial_action": [
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      ],
      "manufacturer_g1_zip_code": "",
      "report_to_manufacturer": "",
      "manufacturer_zip_code_ext": "",
      "manufacturer_g1_name": "",
      "adverse_event_flag": "Y",
      "distributor_address_1": "",
      "manufacturer_state": "",
      "distributor_address_2": "",
      "manufacturer_postal_code": "",
      "single_use_flag": "",
      "manufacturer_country": "",
      "mdr_text": [
        {
          "mdr_text_key": "3507572",
          "text_type_code": "Description of Event or Problem",
          "patient_sequence_number": "1",
          "text": "THE PATIENT CAME TO THE ER IN CARDIAC ARREST AND WAS SUCCESSFULLY RESUSCITATED AND ADMITTED. THE NEXT DAY THE PATIENT WAS IN VENTRICULAR FIBRILLATION AND THE MONITOR DID NOT RECOGNIZE THE RHYTHM NOR DID IT ALARM. RHYTHM WAS RECOGNIZED BY NURSE WHO WAS AT NURSING STATION AND A CODE WAS CALLED.DEVICE #1IS THIS A LABORATORY DEVICE OR LABORATORY TEST?NO."
        }
      ],
      "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": ""
    }
  ]
}