{
  "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": "Charleston",
      "state": "SC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "63255",
      "recalling_firm": "Trumpf Medical Systems, Inc.",
      "address_1": "415 Jessen Ln",
      "address_2": "N/A",
      "postal_code": "29492",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution-USA (nationwide) including the states of AR, CA, CO, CT, FL, GA, IL, KS, MA, MI, MO, NC, NJ, NY, OH, SC, TX, UT, VT and WI.",
      "recall_number": "Z-0077-2013",
      "product_description": "Helion and Xenion surgical lights, 501/01 series KLM lights.     The surgical lights are intended to locally illuminate an operating or examination area of the patient\u0019s body with a high intensity light.",
      "product_quantity": "275 units",
      "reason_for_recall": "Incidents regarding fractures of the front joint of the spring arm have been reported.",
      "recall_initiation_date": "20120919",
      "center_classification_date": "20121018",
      "termination_date": "20140121",
      "report_date": "20121024",
      "code_info": "Ondal AC2000 serial range of the spring arms requiring rework: 0111 010 xxxxxx to 0111 066 xxxxx (010 to 066 = month 01/year 20000 to month 06/year 2006 xxxxxx = 5 digit serial number)."
    }
  ]
}