{
  "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": "2026-04-15",
    "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": "69759",
      "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 Distribution: US (nationwide) including states of: MI, MN, MO, OH, PA, IA, and TN; and  Internationally to:  SWITZERLAND; CANADA, COLOMBIA,  GERMANY, Dubai, (UAE), THAILAND; SOUTH AFRICA,  SOUTH KOREA; and SINGAPORE.",
      "recall_number": "Z-0591-2015",
      "product_description": "LEGION(TM) COCR CONSTRAINED FEMORAL COMPONENT, SIZE 6, LEFT, REF 71426006, QTY 1, Smith & Nephew, knee prosthesis    Usage:orthopedic.",
      "product_quantity": "23 units",
      "reason_for_recall": "The stem taper on this device is undersized; the gauge point is not deep enough.",
      "recall_initiation_date": "20141104",
      "center_classification_date": "20141211",
      "termination_date": "20190822",
      "report_date": "20141217",
      "code_info": "Lot Number 14EM23391"
    }
  ]
}