{
  "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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      "date_changed": "20250813",
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      "manufacturer_contact_city": "",
      "mdr_report_key": "2925088",
      "removal_correction_number": "",
      "number_devices_in_event": "",
      "date_report_to_fda": "20121126",
      "manufacturer_name": "",
      "report_source_code": "User Facility report",
      "remedial_action": [
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      "report_to_manufacturer": "",
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      "mdr_text": [
        {
          "mdr_text_key": "18622173",
          "text_type_code": "Description of Event or Problem",
          "patient_sequence_number": "1",
          "text": "DURING PROCEDURE, ANESTHESIA MACHINE ERROR OCCURRED TWICE PER ATTENDING SURGEON. PATIENT SUPPORTED WITH AMBU BAG WITH SUPPLEMENTAL O2. PROPOFOL GTT WAS INITIATED. MACHINE REPLACED WITH CONTINUOUS MONITORING USING PORTABLE DEVICE. PATIENT VSS THROUGHOUT SURGERY.ATTENDING SURGEON INDICATED THAT THIS PIECE OF EQUIPMENT WAS KNOWN TO HAVE HAD PROBLEMS."
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}