{
  "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": "2026-04-29",
    "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": "66333",
      "recalling_firm": "Smith & Nephew Inc",
      "address_1": "1450 E. Brooks Rd",
      "address_2": "N/A",
      "postal_code": "38116",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Worldwide Distribution - USA including Nevada and Internationally to  United Arab Emirates, Italy, Spain, Belgium, Bulgaria, Poland, France, Japan, Netherlands, Australia, Turkey, Russian Federation, Germany and United Kingdom.",
      "recall_number": "Z-0445-2014",
      "product_description": "GENESIS(R) II, PS HIGH FLEXION ARTICULAR INSERT, SIZE 3-4, 13 MM  QTY: (1), REF 71420820, STERILE EO, Smith & Nephew, Inc. Memphis, TN 38116 USA    Orthopedic",
      "product_quantity": "45 pieces",
      "reason_for_recall": "The Tyvek(TM) lid on one, or both, of the two trays that form a  double barrier around the insert may not have been adequately sealed.",
      "recall_initiation_date": "20130827",
      "center_classification_date": "20131204",
      "termination_date": "20190820",
      "report_date": "20131211",
      "code_info": "Batch No. 12GT20824"
    }
  ]
}