{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Completed",
      "city": "Memphis",
      "state": "TN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90547",
      "recalling_firm": "Smith & Nephew, Inc.",
      "address_1": "1450 E Brooks Rd",
      "address_2": "N/A",
      "postal_code": "38116-1804",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of AZ, CA, GA, KS, LA, MN, MI, MO, MS, NC, NJ, NY, OR, SC, TN, VA, WA, and WI.",
      "recall_number": "Z-1418-2022",
      "product_description": "(1) Genesis II Non-Porous Tibial Baseplate Size 5 Right, Product #71420186.  (2) Genesis II Non-Porous Tibial Baseplate Size 4 Left, Product #71420166.",
      "product_quantity": "31 devices",
      "reason_for_recall": "The product was mispackaged (swapped).  The devices within the inner tray matches the inner tray but does not match the outer box label and the chart sticks.",
      "recall_initiation_date": "20220627",
      "center_classification_date": "20220720",
      "report_date": "20220727",
      "code_info": "Product #71420186 - Lot #21DM14954S, exp. October 2030, UDI #03596010206350.  Product #71420166 - Lot #21FM13870A, exp. October 2030, UDI #03596010206268."
    }
  ]
}