{
  "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": [
    {
      "country": "United States",
      "city": "Memphis",
      "address_1": "1450 E Brooks Rd",
      "reason_for_recall": "The affected products were inadvertently packaged with an incorrect screw component.",
      "address_2": "",
      "product_quantity": "12 units",
      "code_info": "13KSL0038C",
      "center_classification_date": "20190912",
      "distribution_pattern": "Foreign countries of;   France, Germany, Netherlands, Norway, Switzerland",
      "state": "TN",
      "product_description": "LEGION(TM) HEMI STEP TIBIAL WEDGE RK/HK, 5 MM, SIZE 3-4 LT.MDL/RT-LAT, REF 71423432    Product Usage:   The constrained knee systems are designed for use in patients in primary and revision surgery, where the posterior cruciate ligament and one or both of the collateral ligaments (i.e., medial collateral and/or lateral collateral ligament) are absent or incompetent.",
      "report_date": "20190918",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Smith & Nephew, Inc.",
      "recall_number": "Z-2538-2019",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "83596",
      "more_code_info": "",
      "recall_initiation_date": "20180115",
      "postal_code": "38116-1804",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Completed"
    }
  ]
}