{
  "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": "2026-06-11",
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          "patient_problems": [
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          ]
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      "mdr_text": [
        {
          "mdr_text_key": "340103563",
          "text_type_code": "Description of Event or Problem",
          "patient_sequence_number": "0",
          "text": "ANESTHESIA MACHINE FAILED ITS ROUTINE PRE-USE SAFETY CHECK. AIR LEAK OF 171ML. FAULTY MV2 VALVE."
        }
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      "suppl_dates_fda_received": ""
    }
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}