{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Bonaduz",
      "state": "N/A",
      "country": "Switzerland",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91925",
      "recalling_firm": "Hamilton Medical AG",
      "address_1": "Via Crusch 8",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of CA, MA, ID, NC, GA, FL, NV, PA, MO, KS, SC, NY, NM, WY, VA.",
      "recall_number": "Z-1429-2023",
      "product_description": "HAMILTON-C6, REF: 160021",
      "product_quantity": "103",
      "reason_for_recall": "Software error causes, safety ventilation, in which ventilation continues in the \"safety ventilation\" mode with audible/visible alarm - patient inputs are not monitored, if the following coincide 1) A mode change to an adaptive mode (ASV, APVcmv, APVsimv, INTELLiVENT-ASV, (S)CMV+, SIMV+), and 2) The controller and/or humidifier is connected to the ventilator and is operational.",
      "recall_initiation_date": "20230314",
      "center_classification_date": "20230425",
      "report_date": "20230503",
      "code_info": "Software Version: 1.2.1, UDI-DI: 07630002808590"
    }
  ]
}