{
  "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": "2026-04-01",
    "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": "84647",
      "recalling_firm": "Smith & Nephew, Inc.",
      "address_1": "1450 E Brooks Rd",
      "address_2": "",
      "postal_code": "38116-1804",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "USA:  TN, NC, CA,OR, NM, TX, PA, MI, LA, DA, IL.  Int'l:  IT (Italy), NL (Netherlands), RO (Romania), PR (Puerto Rico).",
      "recall_number": "Z-1507-2020",
      "product_description": "LEGION PS High Flex XLPE size 5-6 9mm Articular Insert",
      "product_quantity": "29 units",
      "reason_for_recall": "LEGION PS High Flex XLPE Articular Insert was packaged with an incorrect part",
      "recall_initiation_date": "20191219",
      "center_classification_date": "20200317",
      "termination_date": "20240904",
      "report_date": "20200325",
      "code_info": "Lot Number 19FM12500; Product Number 71453221.",
      "more_code_info": ""
    }
  ]
}