{
  "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": "Two lots of Genesis II Non Porous C/R Femoral Size 6 right packaged were distributed containing Genesis II C/R Femoral Size 4 left.",
      "address_2": "",
      "product_quantity": "27 units",
      "code_info": "Lot Numbers:  16CMB0061A, 16CMB0066A",
      "center_classification_date": "20180822",
      "distribution_pattern": "Australia, Austria, Germany, Great Britain, Poland, Spain",
      "state": "TN",
      "product_description": "GENESIS II NON-POROUS CRUCIATE RETAINING FEMORAL COMPONENT, SIZE 6 RIGHT, REF 71420026  Knee prosthesis",
      "report_date": "20180829",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Smith & Nephew, Inc.",
      "recall_number": "Z-2883-2018",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "80752",
      "termination_date": "20190219",
      "more_code_info": "",
      "recall_initiation_date": "20170801",
      "postal_code": "38116-1804",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}