{
  "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": "2026-08-13",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "130513",
      "product_res_number": "Z-0141-2015",
      "event_date_initiated": "2014-10-09",
      "event_date_posted": "2014-10-27",
      "recall_status": "Terminated",
      "event_date_terminated": "2016-03-23",
      "res_event_number": "69426",
      "product_code": "JEA",
      "product_description": "TITAN Operating Room Table\n\nPatient positioning during surgery, ranging from anesthesia induction to actual surgery to recovery from anesthesia. Patient transport on the operating tabletop, from the patient transfer system to the operating theatre or from the operating theatre to the patient transfer system.",
      "code_info": "TITAN Operating Tables:  1465166, 1228073, 1397903, 4544260.",
      "firm_fei_number": "3003184737",
      "recalling_firm": "Trumpf Medical Systems, Inc.",
      "address_1": "1046 Legrand Blvd",
      "city": "Charleston",
      "state": "SC",
      "postal_code": "29492-7672",
      "additional_info_contact": "Lindsey Ronnenberg\n843-534-0606",
      "reason_for_recall": "Unintended movement of the operating table during surgical cases due to the use of damaged TITAN remotes.",
      "root_cause_description": "Device Design",
      "action": "TRUMPF sent an Urgent Medical Device Correction letter dated October 3, 2014, to all affected customers. The letter identified the product the problem and the action needed to be taken by the customer.\n\nActions to be taken:\n\nComplete and return the attached Confirmation of Receipt form with serial numbers of the TITAN table(s) and the serial number(s) for any remote controls you have. We will then arrange to send replacement remotes, which have been redesigned to eliminate this mode of failure.  You will then be required to dispose of your recalled remotes.\n\nIf you have any questions concerning this request or the procedure as outlined, please contact TRUMPF Medical Systems, Inc. at 888-474-9359.",
      "product_quantity": "184 units",
      "distribution_pattern": "Worldwide Disttribution: US (nationwide) including the states of AL, AZ, CT, FL, GA, IA, IL, IN, KS, MD, MI, MN, MO, NC, ND, NJ, NM, NV, NY, OH, OR, PA, SC, TX, VA, WA and WY: and Internationally to Canada.",
      "openfda": {
        "registration_number": [
          "3012995405",
          "9681642",
          "3010890274",
          "2221819",
          "3013522950",
          "1043572",
          "3007031002",
          "2916273",
          "2921578",
          "9680168",
          "3003923584",
          "3043007473",
          "1000351276",
          "3031563141",
          "3012329926",
          "3007143268",
          "3027847726",
          "1066635",
          "8010652",
          "8043933",
          "3009760038",
          "3013836619",
          "3015223105",
          "3011111237"
        ],
        "fei_number": [
          "1841",
          "3012995405",
          "1000295034",
          "3010890274",
          "2221819",
          "3013522950",
          "1043572",
          "3007031002",
          "2916273",
          "2921578",
          "3003184737",
          "3003923584",
          "3043007473",
          "1000395711",
          "1000351276",
          "3031563141",
          "3012329926",
          "3007143268",
          "3027847726",
          "3009760038",
          "3013836619",
          "3002619595",
          "3015223105",
          "3011111237"
        ],
        "device_name": "Table, Surgical With Orthopedic Accessories, Ac-Powered",
        "medical_specialty_description": "General, Plastic Surgery",
        "regulation_number": "878.4960",
        "device_class": "1",
        "k_number": [
          "K900290",
          "K873079",
          "K953071",
          "K881060",
          "K873080",
          "K924094",
          "K894789",
          "K910736",
          "K911522",
          "K874762"
        ]
      }
    }
  ]
}