{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Completed",
      "city": "Bonaduz",
      "state": "",
      "country": "Switzerland",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90460",
      "recalling_firm": "Hamilton Medical AG",
      "address_1": "Via Crusch 8",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US: WI, FL, CA, NV, PA, TX, PA",
      "recall_number": "Z-1385-2022",
      "product_description": "HAMILTON-H900 Humidifier, Models: 950001, 950004",
      "product_quantity": "203",
      "reason_for_recall": "When starting a humidifier, intended for respiratory gas conditioning during invasive and noninvasive mechanical ventilation, with an empty chamber, and water is not filled into the chamber, the low water level alarm will be delayed and medical staff are unaware that there is no water in the chamber.",
      "recall_initiation_date": "20210105",
      "center_classification_date": "20220714",
      "report_date": "20220720",
      "code_info": "UDI:07630002801546. All devices with software version 1.10c",
      "more_code_info": ""
    }
  ]
}