{
  "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": "Ongoing",
      "city": "Memphis",
      "state": "TN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89031",
      "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": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US Nationwide distribution in the states of CO, FL, GA, MA, MN, MO, NC, NJ, NV, NY, OH, OK, PA, TN, TX, WA.",
      "recall_number": "Z-0365-2022",
      "product_description": "smith&nephew EVOS CONDYLAR MEDIAL DISTAL FEMUR PLATE, L, 5H, 115MM, REF 72573102",
      "product_quantity": "35 units",
      "reason_for_recall": "Testing vendor notified Smith & Nephew that previous MRI scanning conditions provided in Exponent\u0019s reports were erroneous. Erroneous data from the reports was incorporated in the released IFU  81110294 EVOS Large Fragment Plating System.",
      "recall_initiation_date": "20211101",
      "center_classification_date": "20211210",
      "report_date": "20211222",
      "code_info": "Batch Number:  20HM10252, 20HM10253, 20HM10254, 20HM22785, UDI",
      "more_code_info": ""
    }
  ]
}