{
  "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": "2026-09-08",
    "results": {
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      "manufacturer_contact_zip_ext": "4386",
      "manufacturer_g1_address_2": "",
      "event_location": "",
      "report_to_fda": "",
      "manufacturer_contact_t_name": "MR.",
      "manufacturer_contact_state": "CA",
      "manufacturer_link_flag": "Y",
      "manufacturer_contact_address_2": "",
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      "manufacturer_contact_pcity": "85861720",
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      "report_number": "2016493-2022-932174",
      "type_of_report": [
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      "manufacturer_address_2": "",
      "pma_pmn_number": "K133532",
      "date_of_event": "20201029",
      "reprocessed_and_reused_flag": "N",
      "manufacturer_address_1": "",
      "exemption_number": "",
      "manufacturer_contact_zip_code": "92121",
      "reporter_occupation_code": "003",
      "manufacturer_contact_plocal": "8586172000",
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      "manufacturer_g1_postal_code": "921214386",
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      "manufacturer_contact_area_code": "858",
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      "manufacturer_contact_f_name": "BRETT",
      "device_date_of_manufacturer": "20191031",
      "previous_use_code": "U",
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        {
          "device_event_key": "",
          "implant_flag": "",
          "date_removed_flag": "",
          "device_sequence_number": "1204795",
          "implant_date_year": "",
          "date_removed_year": "",
          "serviced_by_3rd_party_flag": "N",
          "date_received": "20220507",
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          "generic_name": "PUMP, INFUSION",
          "manufacturer_d_name": "CAREFUSION SD",
          "manufacturer_d_address_1": "10020 PACIFIC MESA BLVD",
          "manufacturer_d_address_2": "",
          "manufacturer_d_city": "SAN DIEGO",
          "manufacturer_d_state": "CA",
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          "manufacturer_d_zip_code_ext": "4386",
          "manufacturer_d_country": "US",
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          "catalog_number": "8015 ALARIS PCU 1.5 MODULE",
          "lot_number": "",
          "other_id_number": "",
          "device_availability": "Device was returned to manufacturer",
          "date_returned_to_manufacturer": "20201029",
          "device_report_product_code": "FRN",
          "device_age_text": "",
          "device_evaluated_by_manufacturer": "Y",
          "combination_product_flag": "N",
          "udi_di": "10885403801532",
          "udi_public": "10885403801532",
          "openfda": {
            "device_name": "Pump, Infusion",
            "medical_specialty_description": "General Hospital",
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          }
        }
      ],
      "product_problems": [
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        "Application Program Freezes or Fails to Launch"
      ],
      "reporter_state_code": "CA",
      "manufacturer_zip_code": "",
      "suppl_dates_mfr_received": "",
      "mfr_report_type": "Thirty-Day",
      "manufacturer_contact_country": "US",
      "date_changed": "20250728",
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      "manufacturer_contact_extension": "",
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      "manufacturer_contact_phone_number": "8586",
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          "date_received": "20220507",
          "sequence_number_treatment": [
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          ],
          "sequence_number_outcome": [
            ""
          ],
          "patient_age": "",
          "patient_sex": "Unknown",
          "patient_weight": "",
          "patient_ethnicity": "",
          "patient_race": "",
          "patient_problems": [
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            "No Clinical Signs, Symptoms or Conditions"
          ]
        }
      ],
      "distributor_city": "",
      "date_report": "20201029",
      "initial_report_to_fda": "No",
      "distributor_state": "",
      "event_key": "",
      "manufacturer_g1_country": "US",
      "manufacturer_contact_city": "SAN DIEGO",
      "mdr_report_key": "14314988",
      "removal_correction_number": "",
      "number_devices_in_event": "",
      "date_manufacturer_received": "20201029",
      "manufacturer_name": "",
      "report_source_code": "Manufacturer report",
      "remedial_action": [
        ""
      ],
      "manufacturer_g1_zip_code": "92121",
      "report_to_manufacturer": "",
      "manufacturer_zip_code_ext": "",
      "manufacturer_g1_name": "CAREFUSION SD",
      "adverse_event_flag": "N",
      "distributor_address_1": "",
      "manufacturer_state": "",
      "distributor_address_2": "",
      "manufacturer_postal_code": "",
      "single_use_flag": "N",
      "manufacturer_country": "",
      "mdr_text": [
        {
          "mdr_text_key": "299611160",
          "text_type_code": "Additional Manufacturer Narrative",
          "patient_sequence_number": "0",
          "text": "THE INFORMATION PROVIDED WAS OBTAINED FROM A RETROSPECTIVE REVIEW OF SERVICING DATA; THEREFORE, NO OTHER INFORMATION IS OBTAINABLE AT THIS TIME. THERE WAS NO REPORTED PATIENT INVOLVEMENT."
        },
        {
          "mdr_text_key": "299611161",
          "text_type_code": "Description of Event or Problem",
          "patient_sequence_number": "0",
          "text": "IT WAS REPORTED THAT A FAILURE WAS OBSERVED DURING A PLANNED PREVENTIVE MAINTENANCE OR RECALL REMEDIATION SERVICE EVENT. THERE WAS NO REPORTED PATIENT INVOLVEMENT."
        }
      ],
      "number_patients_in_event": "",
      "distributor_name": "",
      "manufacturer_g1_address_1": "10020 PACIFIC MESA BLVD",
      "distributor_zip_code": "",
      "manufacturer_contact_postal_code": "921214386",
      "manufacturer_contact_exchange": "858",
      "manufacturer_contact_pcountry": "",
      "suppl_dates_fda_received": ""
    }
  ]
}