{
  "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": [
    {
      "country": "United States",
      "city": "Houston",
      "address_1": "6721 Portwest Dr Ste 160",
      "reason_for_recall": "The cutting efficiency of the Countersinks was out of specification.",
      "address_2": "",
      "product_quantity": "102 units",
      "code_info": "Lot numbers 1362-01 and 1364-01",
      "center_classification_date": "20150819",
      "distribution_pattern": "US Nationwide Distribution in the states of:  NY, CT, TN, TX, OH, IN, LA, NC, MO, MN, GA, FL, SC, WA, WI, IA, PA, CA, ND, OK, NJ, MI and MD.",
      "state": "TX",
      "product_description": "2.0/2.4 Cannulated Screw Countersink Part # 210-24-002 NON-STERILE and 3.0/4.0 Cannulated Screw Countersink Part # 210-40-002 NON-STERILE       Product Usage:  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.",
      "report_date": "20150826",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Trilliant Surgical Ltd.",
      "recall_number": "Z-2421-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "71783",
      "termination_date": "20170126",
      "more_code_info": "",
      "recall_initiation_date": "20150720",
      "postal_code": "77024-8019",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}