{
  "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": "2026-08-15",
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      "product_res_number": "Z-0155-2014",
      "event_date_initiated": "2013-07-24",
      "event_date_posted": "2013-11-05",
      "recall_status": "Terminated",
      "event_date_terminated": "2014-06-03",
      "res_event_number": "66587",
      "product_code": "JEA",
      "product_description": "ORBIT PT.\n\nThe ORBIT PT works in conjunction with an TRUMPF mobile operating table to automate the patient transport process.",
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      "recalling_firm": "Trumpf Medical Systems",
      "address_1": "1046 Legrand Blvd",
      "city": "Charleston",
      "state": "SC",
      "postal_code": "29492-7672",
      "additional_info_contact": "Lindsey Ronnenberg\n888-474-9359",
      "reason_for_recall": "An odor and smoke developed - The cause was determined to be a power supply unit sitting in the controller column.",
      "root_cause_description": "Component design/selection",
      "action": "The user facility was contacted via phone in early August.  They were contacted 9/17/2013 to schedule the replacement of the power pack because the new power pack became available.",
      "product_quantity": "One",
      "distribution_pattern": "US Distribution: NJ only.",
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