{
  "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": "73609",
      "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": "Letter",
      "distribution_pattern": "International Distribution only in countries of: Germany and Switzerland.",
      "recall_number": "Z-1542-2016",
      "product_description": "TC-PLUS(TM), Primary Fixed Tibial Component VKS Right, SIZE 8 RIGHT, STERILE R, REF 12 000 0012, S&N 7500267, Smith & Nephew Orthopaedics AG    Product Usage: Tibial knee prosthesis",
      "product_quantity": "1 unit",
      "reason_for_recall": "The Affected Devices may contain a dimensional deviation that could potentially result in the  surgeon being unable to seat the polyethylene (PE) Insert on the affected VKS tibial base  plate during surgery.",
      "recall_initiation_date": "20160311",
      "center_classification_date": "20160421",
      "termination_date": "20170410",
      "report_date": "20160427",
      "code_info": "Batch number C1507672"
    }
  ]
}