{
  "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",
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          "udi_public": "",
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      "manufacturer_g1_country": "",
      "date_report_to_manufacturer": "20260306",
      "manufacturer_contact_city": "",
      "mdr_report_key": "24532006",
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      "number_devices_in_event": "",
      "date_report_to_fda": "20260107",
      "manufacturer_name": "",
      "report_source_code": "User Facility report",
      "remedial_action": [
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      "report_to_manufacturer": "",
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      "mdr_text": [
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          "mdr_text_key": "394850327",
          "text_type_code": "Description of Event or Problem",
          "patient_sequence_number": "0",
          "text": "CORRECTION ON THE LAST IRIS REPORT, THE ANESTHESIA MACHINE THAT FAILED DURING THE CASE IS CLINICAL ENGINEERING ID #[REDACTED] AND HAS BEEN MOVED TO [REDACTED] OPERATING ROOM 2."
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      "manufacturer_contact_exchange": "",
      "manufacturer_contact_pcountry": "",
      "suppl_dates_fda_received": ""
    }
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}