{
  "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": "2026-05-06",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Austin",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "62801",
      "recalling_firm": "Encore Medical, Lp",
      "address_1": "9800 Metric Blvd",
      "address_2": "N/A",
      "postal_code": "78758",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution including Venezuela.",
      "recall_number": "Z-2302-2012",
      "product_description": "3DKnee e+ Tibial Insert - HXLPE-VE, Sterile, Material: Highly cross linked vitamin E PE, Sz 2/9mm.    The insert is intended to more closely match the kinematics of the knee, allowing some rotation along the medial condyle and increased congruency along lateral condyle. This insert is to be used along with the other components that comprise the 3DKnee System.",
      "product_quantity": "7 units",
      "reason_for_recall": "The firm is recalling one lot of 392-09-706, 3DKnee e+ Tibial insert, 9 mm, Size 6, Right.  The shelf life labeling of specific lots for a component were found to be incorrect and were found to be expired.",
      "recall_initiation_date": "20120809",
      "center_classification_date": "20120830",
      "termination_date": "20130125",
      "report_date": "20120905",
      "code_info": "Model Number 392-09-706, Lot Number 59602519"
    }
  ]
}