{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Houston",
      "address_1": "15200 Middlebrook Dr",
      "reason_for_recall": "Faded and wrong markings on bone screw Countersink/Depth Gauge instruments in Mini Screw Set.",
      "address_2": "Ste G",
      "product_quantity": "96",
      "code_info": "Mini System part no. IS1100 - lot 0001-0047; Instrument part nos. IS1103, IS1104, and IS1105 - lots 918101, 918102, and 918103",
      "center_classification_date": "20140922",
      "distribution_pattern": "Nationwide: Maine, Oregon, Florida, Texas, Virginia, Arizona, Nebraska, California, Ohio, Illinois, Oklahoma, Washington, North Carolina, Arkansas, Tennessee, New Mexico, Connecticut, Colorado",
      "state": "TX",
      "product_description": "Mini Cannulated Titanium Headed and Headless Screw Set and 2.5, 3.0, and 4.0 mm countersink/depth gauges in the Mini Screw Set/System",
      "report_date": "20141001",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Instratek, Incorporated",
      "recall_number": "Z-2679-2014",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "67727",
      "termination_date": "20160126",
      "recall_initiation_date": "20130425",
      "postal_code": "77058-1216",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}