{
  "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",
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      "cfres_id": "105409",
      "product_res_number": "Z-0398-2012",
      "event_date_initiated": "2011-01-21",
      "event_date_posted": "2012-01-11",
      "recall_status": "Terminated",
      "event_date_terminated": "2012-08-13",
      "res_event_number": "60440",
      "product_code": "FQO",
      "product_description": "OR table TITAN UT, Surgical Table.\n\nSurgical bed with Orthopedic Accessories.",
      "code_info": "Material number 1465166, All Serial numbers.",
      "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 Ronneberg\n843-822-6939",
      "reason_for_recall": "Product is being recalled due to unintended movement on the Titan Tables.",
      "root_cause_description": "Device Design",
      "action": "Trumpf Medical Systems sent an initial notification to customers dated January 24, 2011.  A subsequent \"URGENT SAFETY NOTICE-UPDATE\" letter dated May 26, 2011 was sent to all affected customers.  The letter described the product, problem, and actions to be taken by the customers.  A Corrective Action Plan includes a software update to be installed by a Trumpf Technical Service Representative.  Contact Technical Service at 888-474-9359 for questions regarding this notice.",
      "product_quantity": "see line 1.",
      "distribution_pattern": "Worldwide Distribution.",
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