{
  "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": "Warsaw",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "78372",
      "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": "Letter",
      "distribution_pattern": "OH, MI and TX",
      "recall_number": "Z-0102-2018",
      "product_description": "ROSA Surgical Device 2.5.8.     It is intended to be used in the operating room for the spatial positioning and orientation of an instrument holder or tool guide",
      "product_quantity": "21 (4 US and 17 OUS)",
      "reason_for_recall": "An undetected shift between the information displayed in the navigation software and the actual patient anatomy",
      "recall_initiation_date": "20140214",
      "center_classification_date": "20171116",
      "termination_date": "20200916",
      "report_date": "20171122",
      "code_info": "Serial #s;  RO10009, RO10011, RO10014, and RO13023"
    }
  ]
}