{
  "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": "78944",
      "recalling_firm": "Zimmer Biomet, Inc.",
      "address_1": "56 E Bell Dr",
      "address_2": "N/A",
      "postal_code": "46582-6989",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed to CA, DC, FL, IL, KY, MA, MN, NC, NY, OH, and PA.",
      "recall_number": "Z-0639-2018",
      "product_description": "ROSA Spine 1.0.2 Stereotaxic instrument Computer-assisted surgical device.    Intended for the spatial positioning and orientation of instrument holders to be used by surgeons.",
      "product_quantity": "1",
      "reason_for_recall": "Robot arm being sent to the wrong position",
      "recall_initiation_date": "20170501",
      "center_classification_date": "20180216",
      "termination_date": "20200713",
      "report_date": "20180228",
      "code_info": "SP16008"
    }
  ]
}