{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "West Chester",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79698",
      "recalling_firm": "Synthes, Inc.",
      "address_1": "1302 Wrights Ln E",
      "address_2": "N/A",
      "postal_code": "19380-3417",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution: US (nationwide) and to countries of: Canada and Switzerland.",
      "recall_number": "Z-1514-2018",
      "product_description": "Stem Extractor f/Guide Bar, Part number 03.401.072.  Instrumentation for extraction and revision of Epoca shoulder implants.",
      "product_quantity": "31",
      "reason_for_recall": "There is a potential for the connection screw of the stem extractor to break.",
      "recall_initiation_date": "20180319",
      "center_classification_date": "20180425",
      "termination_date": "20190411",
      "report_date": "20180502",
      "code_info": "09-6793, 10-2637, 10-5070, 12-2707, 14-1085, 15-8949"
    }
  ]
}