{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "cfres_id": "113112",
      "product_res_number": "Z-0077-2013",
      "event_date_initiated": "2012-09-19",
      "event_date_posted": "2012-10-18",
      "recall_status": "Terminated",
      "event_date_terminated": "2014-01-21",
      "res_event_number": "63255",
      "product_code": "FSY",
      "k_numbers": [
        "K011693"
      ],
      "product_description": "Helion and Xenion surgical lights, 501/01 series KLM lights. \n\nThe surgical lights are intended to locally illuminate an operating or examination area of the patients body with a high intensity light.",
      "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).",
      "firm_fei_number": "3003184737",
      "recalling_firm": "Trumpf Medical Systems, Inc.",
      "address_1": "415 Jessen Ln",
      "city": "Charleston",
      "state": "SC",
      "postal_code": "29492",
      "additional_info_contact": "Lindsey Ronnenberg\n843-534-0606",
      "reason_for_recall": "Incidents regarding fractures of the front joint of the spring arm have been reported.",
      "root_cause_description": "Device Design",
      "action": "Trumpf sent an \"URGENT RECALL NOTICE\" dated September 19, 2012 to all affected customers.  The letter identified the product, problem, and actions to be taken by the customers.  A Confirmation of Receipt Form was attached for customers to complete and return.  Contact the firm at 888-474-9359 for questions regarding this notice.",
      "product_quantity": "275 units",
      "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.",
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        "device_name": "Light, Surgical, Ceiling Mounted",
        "medical_specialty_description": "General, Plastic Surgery",
        "regulation_number": "878.4580",
        "device_class": "2"
      }
    }
  ]
}