{
  "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": "71530",
      "recalling_firm": "Zimmer, Inc.",
      "address_1": "1800 W Center St",
      "address_2": "N/A",
      "postal_code": "46580-2304",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Worldwide distribution.  US states of NC and AK; Taiwan, Japan, and Germany.",
      "recall_number": "Z-2060-2015",
      "product_description": "ZNN Antegrade Femoral Nail (ZNN AF).  Orthopedic internal fixation device.",
      "product_quantity": "8",
      "reason_for_recall": "A single distributed ZNN Greater Trochanter Femoral Nail may have been dented.  Potential for fatigue of implant prior to sufficient fracture healing, which may result in need for implant removal and revision of fracture fixation to assure proper healing and avoid fracture malunion or nonunion.",
      "recall_initiation_date": "20150617",
      "center_classification_date": "20150713",
      "termination_date": "20160315",
      "report_date": "20150722",
      "code_info": "Part 47-2492-320-10; lot 62763724",
      "more_code_info": ""
    }
  ]
}