{
  "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": "Morrisville",
      "address_1": "1711 S Pennsylvania Ave",
      "reason_for_recall": "Small Bone Innovations (SBI) is recalling non-sterile RingFIX Olive Wires labeled as item #451-3004 Drill tip 1.8 mm diameter 400mm olive k-wire packaged with item #451-3005 Bayonet tip 1.8mm diameter 400mm olive k-wire inside.",
      "address_2": "",
      "product_quantity": "44",
      "code_info": "item #451-3004,  lot V3R0R.",
      "center_classification_date": "20140604",
      "distribution_pattern": "US Nationwide Distribution in the states of IN, NC, WA, NH, and CT.",
      "state": "PA",
      "product_description": "SBi RingFix Olive Wires    Product Usage:  These are temporary devices indicated for: osteosynthesis of fractures with small osteoarticular fragments, fixation of open and closed fractures, arthrodesis, sepsis, limb lengthening, and osteotomy.",
      "report_date": "20140611",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Small Bone Innovations, Inc.",
      "recall_number": "Z-1720-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "68039",
      "termination_date": "20141020",
      "more_code_info": "",
      "recall_initiation_date": "20140407",
      "postal_code": "19067-2507",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}