{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Reno",
      "state": "NV",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71234",
      "recalling_firm": "Hamilton Medical, Inc.",
      "address_1": "4990 Energy Way",
      "address_2": "N/A",
      "postal_code": "89502-4123",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution",
      "recall_number": "Z-2057-2015",
      "product_description": "Hamilton-G5 Ventilators with software versions V2.40/2.41  Catalog numbers for G5: 159001 and 159002. Software: 159700..  Intensive care ventilation of adult and pediatric patients and optionally infant and neonatal patients.",
      "product_quantity": "248",
      "reason_for_recall": "Customer reports that the ventilator display can freeze. Ventilation continues but the information is no longer displayed on the screen and the user can no longer operate the device.",
      "recall_initiation_date": "20150324",
      "center_classification_date": "20150724",
      "termination_date": "20151223",
      "report_date": "20150805",
      "code_info": "Software version 2.20 and 2.41,"
    }
  ]
}