{
  "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": "2026-05-12",
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      "date_changed": "20250806",
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      "patient": [
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          "date_received": "20120727",
          "sequence_number_treatment": [
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          ],
          "sequence_number_outcome": [
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          ],
          "patient_age": "63 YR",
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        }
      ],
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      "manufacturer_g1_country": "",
      "manufacturer_contact_city": "",
      "mdr_report_key": "2679065",
      "removal_correction_number": "",
      "number_devices_in_event": "",
      "manufacturer_name": "",
      "report_source_code": "Voluntary report",
      "remedial_action": [
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      "mdr_text": [
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          "mdr_text_key": "15861512",
          "text_type_code": "Description of Event or Problem",
          "patient_sequence_number": "1",
          "text": "PT HAD UNDERGONE EXPLORATORY LAPAROTOMY. AT CONCLUSION OF CASE WITH PRESSURE RELIEF VALVE - APL- TURNED TO MINIMUM PRESSURE ABOUT 20 MMHG REMAINED IN CIRCUIT. AS A RESULT, PT COULD NOT ACHIEVE SPONTANEOUS RESPIRATIONS AND PT SUSTAINED DESATURATION. UPON INVESTIGATION EXTENSIVE MOLD AND CONTAMINATION WAS DISCOVERED THROUGHOUT EXPIRATORY SIDE OF ANESTHESIA CIRCUIT. ANESTHESIA MACHINE INVOLVED WAS A DATEX OHMEDA S/5 AVANCE, SERIAL NUMBER (B)(4)."
        }
      ],
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      "manufacturer_contact_exchange": "",
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      "suppl_dates_fda_received": ""
    }
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}