{
  "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": "727 N Shepherd Dr Ste 100",
      "reason_for_recall": "Firm is voluntarily recalling cannulated driver handles (210-00-003 and 210-00-004) that may demonstrate a degradation of function with the adapter collar sticking, and/or not retaining the mating adapter male shaft.",
      "address_2": "",
      "product_quantity": "90",
      "code_info": "Lot: 603600",
      "center_classification_date": "20180702",
      "distribution_pattern": "U.S. States: NE, MA, GA, TX, OR, AZ, FL, OH, WA, NJ, UT, VA, CA, MN, PA, DE, OK, KS, WI, MT, IA, MO",
      "state": "TX",
      "product_description": "Ratcheting Cannulated Driver Handle, Catalog #: 210-00-004, Rx Only, Non Sterile",
      "report_date": "20180711",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Trilliant Surgical Ltd.",
      "recall_number": "Z-2339-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "80195",
      "termination_date": "20200604",
      "more_code_info": "",
      "recall_initiation_date": "20180327",
      "postal_code": "77007-1320",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}