{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Gainesville",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "77592",
      "recalling_firm": "Exactech, Inc.",
      "address_1": "2320 NW 66th Ct",
      "address_2": "N/A",
      "postal_code": "32653-1630",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Distribution to the states of : AZ, CA, CO, FL, IL, OH, OK, NV, NY, SC and TN.",
      "recall_number": "Z-3018-2017",
      "product_description": "Truliant Tibial Trial Handle.    To assist the surgeon in the implantation of Truliant Knee system components according to a conventional technique for total knee replacement. Specifically, these instruments are reusable, surgically invasive, and intended for transient use.t Tibial Trial Handle",
      "product_quantity": "68 devices",
      "reason_for_recall": "The Truliant Tibial Trial Handle's pin may disassociate from the main body.",
      "recall_initiation_date": "20170623",
      "center_classification_date": "20170811",
      "termination_date": "20201130",
      "report_date": "20170823",
      "code_info": "Catalog Number 02-029-29-1000, Lot Number 83843-001."
    }
  ]
}