{
  "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,
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    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Plainsboro",
      "address_1": "311 Enterprise Dr",
      "reason_for_recall": "Through the investigation of reported complaints Integra verified that there have been instances where the Universal Wire Fixation Bolts the Slotted Post broke during use at the surgical site.",
      "address_2": "",
      "product_quantity": "495 units",
      "code_info": "Lot # GT0420 and GT0419",
      "center_classification_date": "20160811",
      "distribution_pattern": "US Distribution to the states of : FL, VA, OK, CO, DC and IN.",
      "state": "NJ",
      "product_description": "Integra External Fixation System Universal Wire Fixation Bolt - 17.5 mm Catalogue #12224218 ; Integra External Fixation System Universal Wire Fixation Bolt - 23 mm Catalogue #12224219",
      "report_date": "20160817",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Integra LifeSciences Corp.",
      "recall_number": "Z-2386-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "74757",
      "termination_date": "20161216",
      "more_code_info": "",
      "recall_initiation_date": "20160720",
      "postal_code": "08536-3344",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}