{
  "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": "Buccinasco",
      "state": "N/A",
      "country": "Italy",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76367",
      "recalling_firm": "Villa Sistemi Medicali S.P.A.",
      "address_1": "Via delle Azalee 3",
      "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 AL, AZ, CA, CO, CT, DC, FL, IA, IL, IN, LA, MA, MD, MI, MN, MO, MS, NJ, NY, PA,   Puerto Rico, TN, TX, UT, and W.I",
      "recall_number": "Z-1429-2017",
      "product_description": "Apollo DRF; Model: 9784220831    Product Usage:  General, multi-function x-ray systems capable of routine radiographs and general fluoroscopy procedures",
      "product_quantity": "65 devices in total",
      "reason_for_recall": "Patient fell from the table because the footrest of the device detached from the table top while the patient was positioned on the table and table was moving from vertical position.",
      "recall_initiation_date": "20161227",
      "center_classification_date": "20170309",
      "termination_date": "20210309",
      "report_date": "20170315",
      "code_info": "08090531  09090591  10040680  15051450  11020798"
    }
  ]
}