{
  "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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      "event_location": "INVALID DATA",
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      "date_added": "19950306",
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          "brand_name": "TRANSFER CHAMBER",
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          "manufacturer_d_name": "SIM/INTEC",
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          "manufacturer_d_country": "",
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          "model_number": "",
          "catalog_number": "9000",
          "lot_number": "8382 (SUSPECT MORE THAN 1 LOT#",
          "other_id_number": "",
          "device_operator": "INVALID DATA",
          "device_availability": "No answer provided",
          "device_report_product_code": "",
          "device_age_text": "",
          "device_evaluated_by_manufacturer": "",
          "baseline_510_k__flag": "",
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          "openfda": {}
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      "date_changed": "20250729",
      "health_professional": "",
      "summary_report_flag": "N",
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      "manufacturer_contact_phone_number": "",
      "patient": [
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          "date_received": "19940805",
          "sequence_number_treatment": [
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          "patient_age": "UNK",
          "patient_sex": "",
          "patient_weight": "",
          "patient_ethnicity": "",
          "patient_race": ""
        }
      ],
      "distributor_city": "",
      "date_report": "19940728",
      "initial_report_to_fda": "",
      "distributor_state": "",
      "event_key": "",
      "manufacturer_g1_country": "",
      "manufacturer_contact_city": "",
      "mdr_report_key": "10000",
      "removal_correction_number": "",
      "number_devices_in_event": "",
      "manufacturer_name": "",
      "report_source_code": "User Facility report",
      "remedial_action": [
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      "adverse_event_flag": "*",
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      "manufacturer_state": "",
      "distributor_address_2": "",
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      "single_use_flag": "",
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      "mdr_text": [
        {
          "mdr_text_key": "5377",
          "text_type_code": "Description of Event or Problem",
          "patient_sequence_number": "1",
          "text": "ONE OR MORE CRACKS IN GREY PLASTIC SURROUNDING FILTER MATERIAL.  WATER FLOWS THROUGH THESE CRACKS, FILLS THE CHAMBER AND CAUSES THE HEATER TO HEAT IMPROPERLY.INVALID DATA - REGARDING SINGLE USE LABELING OF DEVICE.  PATIENT MEDICAL STATUS PRIOR TO EVENT:  INVALID DATA.  INVALID DATA - REGARDING MULTIPLE PATIENT INVOLVEMENT.INVALID DATA - ON DEVICE SERVICE/MAINTENANCE.  NO DATA - REGARDING DATE LAST SERVICED.  SERVICE PROVIDED BY:  INVALID DATA.  INVALID DATA - SERVICE RECORDS AVAILABILITY.INVALID DATA - REGARDING WHETHER EVENT PRESENTS IMMINENT HAZARD.  INVALID DATA - WHETHER DEVICE USED AS LABELED/INTENDED.INVALID DATA - REGARDING EVALUATION BY USER AFTER EVENT.  METHOD OF EVALUATION:  INVALID DATA.  RESULTS OF EVALUATION:  INVALID DATA.  CONCLUSION:  INVALID DATA.  CERTAINTY OF DEVICE AS CAUSE OF OR CONTRIBUTOR TO EVENT:  INVALID DATA.  CORRECTIVE ACTIONS:  NO DATA.  INVALID DATA - ON DEVICE DESTROYED/DISPOSED OF STATUS."
        }
      ],
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      "distributor_name": "",
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      "distributor_zip_code": "",
      "manufacturer_contact_postal_code": "",
      "manufacturer_contact_exchange": "",
      "manufacturer_contact_pcountry": "",
      "suppl_dates_fda_received": ""
    }
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}