{
  "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": [
    {
      "country": "United States",
      "city": "Warsaw",
      "address_1": "1800 W Center St",
      "reason_for_recall": "Complaints have been reported that the handpiece is inoperable. The investigation found that the complaints were related to the lack of preventative maintenance contrary to what is recommended in the instructions for use included with the handpiece. An inoperable device may lead to a delay in surgery",
      "address_2": "",
      "product_quantity": "703",
      "code_info": "Item Number  00-5927-040-00  Serial Number  All",
      "center_classification_date": "20161026",
      "distribution_pattern": "Nationwide.  CANADA  HONG KONG  KOREA  SINGAPORE  CHINA  VENEZUELA  AUSTRALIA  JAPAN  NETHERLANDS  GERMANY  INDIA  TAIWAN",
      "state": "IN",
      "product_description": "Zimmer¿ Gender Solutions\" Patellofemoral Joint Prosthesis  Milling Handpiece",
      "report_date": "20161102",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer Biomet, Inc.",
      "recall_number": "Z-0317-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "75371",
      "termination_date": "20200416",
      "more_code_info": "",
      "recall_initiation_date": "20160928",
      "postal_code": "46580-2304",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}