{
  "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": "2026-04-29",
    "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": "65738",
      "recalling_firm": "Smith & Nephew Inc",
      "address_1": "1450 E. Brooks Rd",
      "address_2": "N/A",
      "postal_code": "38116",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "International only:  Germany, France, United Arab Emirates, and United Kingdom.",
      "recall_number": "Z-1996-2013",
      "product_description": "GENESIS(R) II CRUCIATE RETAINING ARTICULAR INSERT, TRIAL, SIZE 3-4, A/P 48 MM, M/L 68 MM, QTY 1, NON-STERILE, REF 71430490,     Product Usage:  Orthopedic",
      "product_quantity": "9 units",
      "reason_for_recall": "The products were produced using the wrong color material, resulting in the devices  being red (used for deep dished inserts) instead of blue (used for cruciate retaining inserts).",
      "recall_initiation_date": "20130708",
      "center_classification_date": "20130821",
      "termination_date": "20190819",
      "report_date": "20130828",
      "code_info": "Lot Number 12LM03798"
    }
  ]
}