{
  "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": [
    {
      "status": "Terminated",
      "city": "Plainsboro",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "63856",
      "recalling_firm": "Integra LifeSciences Corp.",
      "address_1": "311 Enterprise Dr",
      "address_2": "N/A",
      "postal_code": "08536-3344",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed in the states of IL, ID, LA, MA, NJ, NY, OH, PA, and SD.",
      "recall_number": "Z-1103-2013",
      "product_description": "Integra XKnife¿ Stereotactic Radiosurgery and Radiotherapy Treatment Planning,  Software Versions 5.0.1 and 5.0.2.    Intended for use in stereotactic and non-stereotactic (frameless stereotactic), collimated beam, computer planned, linear accelerator (Linac) based treatment.",
      "product_quantity": "11 XKnife V5.0.1  and 1 XKnife V5.0.2",
      "reason_for_recall": "Depending on the system configuration, a software error message in versions 5.0.1 and 5.0.2. occurs if a beam plan is transmitted from XKnife using DICOM-RT.",
      "recall_initiation_date": "20121210",
      "center_classification_date": "20130412",
      "termination_date": "20130801",
      "report_date": "20130424",
      "code_info": "Software Versions 5.0.1 and 5.0.2."
    }
  ]
}