{
  "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": "West Chester",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "66418",
      "recalling_firm": "Synthes USA HQ, 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 - USA including ID, FL, TN, NY, LA and Internationally to Canada.",
      "recall_number": "Z-0409-2014",
      "product_description": "Synthes 4.5 mm LCP Curved Condylar Plate     Intended for buttressing multifragmentary distal femur fractures.",
      "product_quantity": "13",
      "reason_for_recall": "The Synthes 4.5 mm LCP Curved Condylar Plate was recalled because a Straight Condylar Plate is etched with a Curved Condylar Plate part number.",
      "recall_initiation_date": "20130730",
      "center_classification_date": "20131126",
      "termination_date": "20150831",
      "report_date": "20131204",
      "code_info": "Part No. 02.001.324, lot no. 6900823"
    }
  ]
}