{
  "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": "Memphis",
      "state": "TN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "78840",
      "recalling_firm": "Smith & Nephew, Inc.",
      "address_1": "1450 E Brooks Rd",
      "address_2": "N/A",
      "postal_code": "38116-1804",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Worldwide",
      "recall_number": "Z-0409-2018",
      "product_description": "Smith & Nephew Taylor Spatial Frame Website software, Catalog Number 71070401.  A web-based and mobile application software component of a multilateral external fixation system that is intended for fracture fixation, fixation of long bones and for joint fusions and limb lengthening or deformity corrections which involve cutting of the bone.",
      "product_quantity": "N/A",
      "reason_for_recall": "In rare circumstances, when surgeons use the software to plan the strut adjustment, an  inverted  image of the frame is generated by the software. The frame will appear  inverted  in the preview images on the Strut Settings tab.",
      "recall_initiation_date": "20171213",
      "center_classification_date": "20180124",
      "termination_date": "20201005",
      "report_date": "20180131",
      "code_info": "Version 5.2.5 and 5.2.6"
    }
  ]
}