{
  "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": [
    {
      "country": "United States",
      "city": "Arlington",
      "address_1": "11576 Memphis Arlington Rd",
      "reason_for_recall": "The firm discovered a lack of adequate documentation confirming sterility on certain products.",
      "address_2": "",
      "product_quantity": "40 units",
      "code_info": "Lot Number 1568030",
      "center_classification_date": "20191125",
      "distribution_pattern": "US and Norway, Italy, Germany, France, South Africa, UK, Taiwan, Austria, Japan, Turkey, Denmark, Canada, Switzerland, Belgium, The Netherlands, Spain",
      "state": "TN",
      "product_description": "ORTHOLOC 3DI PLT SYS STERILE, LOCKING SCREW, 3.5 x 38mm Sterile, Part Number 58S03538",
      "report_date": "20191204",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Wright Medical Technology, Inc.",
      "recall_number": "Z-0563-2020",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "84180",
      "termination_date": "20201103",
      "more_code_info": "",
      "recall_initiation_date": "20161108",
      "postal_code": "38002-9497",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}