{
  "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": "93284",
      "product_res_number": "Z-0166-2011",
      "event_date_initiated": "2010-03-31",
      "event_date_posted": "2010-10-28",
      "recall_status": "Terminated",
      "event_date_terminated": "2012-03-01",
      "res_event_number": "56352",
      "product_code": "JAI",
      "k_numbers": [
        "K050422"
      ],
      "product_description": "Siemens brand 550 TxT Patient Table, Part No. 7346534, Distributed by and/or Manufactured by Siemens AG, Medical Solutions, Germany",
      "code_info": "All codes.",
      "firm_fei_number": "2937457",
      "recalling_firm": "Siemens Medical Solutions USA,  Inc",
      "address_1": "4040 Nelson Ave",
      "city": "Concord",
      "state": "CA",
      "postal_code": "94520-1200",
      "additional_info_contact": "Christine Dunbar\n925-246-8407",
      "reason_for_recall": "An increase in voltage may cause a short circuit of a power transistor that may cause a smoldering and smoking effect of the electrical wiring and also an unexpected lowering of the Table. Both issues present the potential for injury to a patient or the operator.",
      "root_cause_description": "Other",
      "action": "Siemens sent a Customer Information Letter on March 31, 2010, to all consignees.  The letter identified the product, the problem, and the action that should be taken.  Siemens implemented minor modifications to address the issues.  No further action was required for the continual operation of the 550TxT Table.  \nFor questions regarding this recall call 925-602-8083.",
      "product_quantity": "326 units",
      "distribution_pattern": "Worldwide Distribution including USA",
      "openfda": {
        "k_number": [
          "K231612",
          "K072898",
          "K910002",
          "K122201",
          "K060671",
          "K910971",
          "K855063",
          "K834201",
          "K050422",
          "K120916",
          "K910648",
          "K062639",
          "K170502",
          "K983678",
          "K982446",
          "K837152",
          "K182683",
          "K993522",
          "K071870",
          "K031866",
          "K013036",
          "K033316",
          "K160518",
          "K041448",
          "K122413",
          "K120520",
          "K042146",
          "K034054",
          "K941927",
          "K964740",
          "K060870",
          "K132084"
        ],
        "registration_number": [
          "9710332",
          "3015232217",
          "2247992",
          "3006894636",
          "2436865",
          "3006946288",
          "3012834372",
          "1932738"
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          "3015232217",
          "3006894636",
          "1000143606",
          "1000521490",
          "3006946288",
          "1000208827",
          "3012834372"
        ],
        "device_name": "Couch, Radiation Therapy, Powered",
        "medical_specialty_description": "Radiology",
        "regulation_number": "892.5770",
        "device_class": "2"
      }
    }
  ]
}