{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Tucson",
      "state": "AZ",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "75600",
      "recalling_firm": "SynCardia Systems Inc.",
      "address_1": "1992 E Silverlake Rd",
      "address_2": "N/A",
      "postal_code": "85713-3865",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "US distribution to Virginia and Arizona.",
      "recall_number": "Z-0659-2017",
      "product_description": "5000 Series Freedom Drivers.  Freedom Driver System for Temporary Total Artificial Heart (TAH-t).  Part number 595000-001",
      "product_quantity": "5",
      "reason_for_recall": "The Main Printed Circuit Board Assembly (PCBA) of the affected Freedom Drivers may fail and cause the Freedom Driver to stop functioning without visual or audible alarms, resulting in the loss of life-sustaining function.",
      "recall_initiation_date": "20161021",
      "center_classification_date": "20161208",
      "termination_date": "20170221",
      "report_date": "20161214",
      "code_info": "S/N 5002 \u0013 UDI (01)00858000003121(21)5002  S/N 5005 \u0013 UDI (01)00858000003121(21)5005  S/N 5008 \u0013 UDI (01)00858000003121(21)5008  S/N 5009 \u0013 UDI (01)00858000003121(21)5009  S/N 5010 \u0013 UDI (01)00858000003121(21)5010"
    }
  ]
}