{
  "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": "77672",
      "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": "AR, OH, MI, and TX",
      "recall_number": "Z-0178-2018",
      "product_description": "ROSA Surgical Device 2.5.8",
      "product_quantity": "22 units (4 US and 18 OUS)",
      "reason_for_recall": "Issue with optional neuro-endoscopy module detected under specific conditions during internal testing.",
      "recall_initiation_date": "20130210",
      "center_classification_date": "20171128",
      "termination_date": "20200609",
      "report_date": "20171206",
      "code_info": "Serial No. RO10011, RO10014, RO13023 and RO13027"
    }
  ]
}