{
  "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": "Four lots of Tiger Screw Sterilization Tray Base Assemblies were released to the field with a printing error where k-wire description markings indicate diameters of 0.45 and 0.35 instead of 0.045\" and 0.035\", respectively.",
      "address_2": "",
      "product_quantity": "50 units",
      "code_info": "Lot: TSL003191, TSL003637, TSL004101, TSL004395",
      "center_classification_date": "20170106",
      "distribution_pattern": "Nationwide Distribution",
      "state": "TX",
      "product_description": "Tiger Screw Sterilization Tray Base Assembly Model 210-00-001 Revision N, O  The product is a component of a system indicated for the fixation of fractures, non-unions, arthrodeses, and osteotomies of bones appropriate for the size of the device.",
      "report_date": "20170118",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Trilliant Surgical Ltd.",
      "recall_number": "Z-0960-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "76029",
      "termination_date": "20170517",
      "more_code_info": "",
      "recall_initiation_date": "20161208",
      "postal_code": "77024-8019",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}