{
  "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": "66545",
      "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": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "USA Nationwide Distribution in the states of: AZ, NC, IA, PA, OH, MD, and TN.",
      "recall_number": "Z-0131-2014",
      "product_description": "GENESIS(R) II, NON-POROUS TIBIAL BASE, SIZE 6, RIGHT, QTY: (1), REF 71420188.    Product Usage:  orthopaedic",
      "product_quantity": "4 units",
      "reason_for_recall": "Swapped product.  Non-porous tibial base size 5 L was mis-packaged as size 6 R and vice versa.",
      "recall_initiation_date": "20131007",
      "center_classification_date": "20131101",
      "termination_date": "20160823",
      "report_date": "20131113",
      "code_info": "Batch No. 13GM09505"
    }
  ]
}