{
  "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": "66417",
      "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": "Nationwide Distribution including IL, CA, AZ, FL, TX, UT, VA, NY, NM, and MT.",
      "recall_number": "Z-0452-2014",
      "product_description": "Titanium Trochanteric Fixation Nail (TFN)System    Intended to treat stable and unstable fractures of the proximal femur.",
      "product_quantity": "17",
      "reason_for_recall": "Two lots of Titanium Trochanteric Fixation Nail (TFN) System are missing the second bend in the nail.",
      "recall_initiation_date": "20130730",
      "center_classification_date": "20131204",
      "termination_date": "20150910",
      "report_date": "20131211",
      "code_info": "Part # 456.391S with lot numbers 5536930, exp. 5/20/2016,  and 7161401, exp. 12/31/2021."
    }
  ]
}