{
  "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": "Warsaw",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "77742",
      "recalling_firm": "Zimmer Biomet, Inc.",
      "address_1": "1800 W Center St",
      "address_2": "N/A",
      "postal_code": "46580-2304",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Visit",
      "distribution_pattern": "Worldwide Distribution - US (DC) and Internationally to   Australia and France.",
      "recall_number": "Z-0105-2018",
      "product_description": "ROSA Brain 3.0  Intended for the spatial positioning and orientation of instrument holders or tool guides to be used by neurosurgeons to guide standard neurosurgical instruments. The device is indicated for any neurosurgical procedure in which the use of stereotactic surgery may be inappropriate.",
      "product_quantity": "3 units",
      "reason_for_recall": "Insufficient amount of washers in the Telescopic Arm, allowing some movement of the device.",
      "recall_initiation_date": "20160527",
      "center_classification_date": "20171117",
      "termination_date": "20200616",
      "report_date": "20171129",
      "code_info": "Serial No. BR16004, BR15002, and BR15003"
    }
  ]
}