{
  "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": "Hsinchu",
      "state": "",
      "country": "Taiwan",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76540",
      "recalling_firm": "United Orthopedic Corporation",
      "address_1": "No. 57 Park Avenue 2, Science Park",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Worldwide Distribution - US including State of CA and Internationally to Pakistan, Spain, and Taiwan.",
      "recall_number": "Z-1692-2017",
      "product_description": "UOC Femoral Driver, Product number PE 93045101, orthopedic manual surgical instrument/accessory for use during surgery to implant femoral components and femoral trial, and to remove femoral trial.",
      "product_quantity": "33 units",
      "reason_for_recall": "The locking lever pin component of the femoral driver may become deformed and break, resulting in malfunction during surgery and causing the device to become inoperable.",
      "recall_initiation_date": "20170210",
      "center_classification_date": "20170329",
      "termination_date": "20170628",
      "report_date": "20170405",
      "code_info": "Lot numbers T16A178A (17 units); T16A178B (1 unit), T16A178B1 (3 units); T16A178C (12 units)",
      "more_code_info": ""
    }
  ]
}