{
  "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": "Houston",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71812",
      "recalling_firm": "Trilliant Surgical Ltd.",
      "address_1": "6721 Portwest Dr Ste 160",
      "address_2": "N/A",
      "postal_code": "77024-8019",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution including NY, TX, OH, IN, FL, NH, MN, SC, OK, NJ, CA, NC, MO, GA, WI, IA, TN, WA, and Puerto Rico.",
      "recall_number": "Z-2452-2015",
      "product_description": "3.0/4.0 Cannulated Drill Bit; a component of the Tiger Cannulated Screw System  The Tiger Cannulated Screw Fixation System implants are intended for fixation of fractures, non-unions, arthrodesis and osteotomies of the small bones in the hand and foot. The implants and guide wires are intended for single use only.",
      "product_quantity": "121 units",
      "reason_for_recall": "The cannulation of the 3.0/4.0 Cannulated Drill Bit inner diamter is too small to allow for the guide wire to pass completely through.",
      "recall_initiation_date": "20150720",
      "center_classification_date": "20150824",
      "termination_date": "20170126",
      "report_date": "20150902",
      "code_info": "Lot 1363-01"
    }
  ]
}