{
  "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": "67390",
      "recalling_firm": "Synthes, Inc.",
      "address_1": "1302 Wrights Ln E",
      "address_2": "",
      "postal_code": "19380-3417",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution-USA (nationwide) and the countries of Canada and Switzerland.",
      "recall_number": "Z-0986-2014",
      "product_description": "Synthes 3.2 mm Guide Wire 400mm.    Used for guiding the TFN Helical Blade and TFN Lag Screw into the femoral.",
      "product_quantity": "1,132,096",
      "reason_for_recall": "Synthes 3.2 mm Guide Wire 400mm included an incorrect raw material listed on the label.",
      "recall_initiation_date": "20140127",
      "center_classification_date": "20140216",
      "termination_date": "20151218",
      "report_date": "20140226",
      "code_info": "part No. 357.399 with all lot numbers 4440270 through 49991803, 5000218 through 5894644, 6000409 through 6999404, 7000143 through 7531836, UK09636, UK10233, UK10510, UL11099, and UL11333.",
      "more_code_info": ""
    }
  ]
}