{
  "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": "Davie",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "77553",
      "recalling_firm": "Mako Surgical Corporation",
      "address_1": "2555 Davie Rd Ste 110",
      "address_2": "N/A",
      "postal_code": "33317-7424",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed to the states of AZ, CA, CO, CT, FL, GA, ID, LA, MA, MO, MS, NC, OH, PA, TN, TX, & WA.",
      "recall_number": "Z-2741-2017",
      "product_description": "MAKO RIO Standard System, internal cPCI Card CageP/N: 201337.    Intended to assist the surgeon in providing software defined spatial boundaries during orthopedic procedures.",
      "product_quantity": "20",
      "reason_for_recall": "An intermittent electrical problem that could lead to a loss of system power due to a loose screw connection.",
      "recall_initiation_date": "20170607",
      "center_classification_date": "20170718",
      "termination_date": "20200616",
      "report_date": "20170726",
      "code_info": "Lot No. 05212015"
    }
  ]
}