{
  "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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          "manufacturer_d_country": "US",
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          "lot_number": "",
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          "device_evaluated_by_manufacturer": "",
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      "date_changed": "20250728",
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          ],
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          "patient_ethnicity": "",
          "patient_race": "",
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          ]
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      "mdr_report_key": "1009131",
      "removal_correction_number": "",
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      "report_to_manufacturer": "",
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      "adverse_event_flag": "N",
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      "manufacturer_state": "",
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      "single_use_flag": "",
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      "mdr_text": [
        {
          "mdr_text_key": "19965975",
          "text_type_code": "Description of Event or Problem",
          "patient_sequence_number": "1",
          "text": "MAQUET SERVO I VENTILATOR STOPPED FUNCTIONING AND DID NOT ALARM WHILE VENTILATING HOSPITAL ICU PT. LUCKILY, RESP THERAPIST WAS IN THE ROOM AT TIME OF EVENT, SO NO HARM TO PT. DESIGN FLAW. FAILURE TO ALARM WHEN EQUIPMENT FAILED."
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      "manufacturer_contact_exchange": "",
      "manufacturer_contact_pcountry": "",
      "suppl_dates_fda_received": ""
    }
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}