{
  "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",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "35602",
      "product_res_number": "Z-0269-05",
      "event_date_initiated": "2004-10-21",
      "event_date_posted": "2005-02-24",
      "recall_status": "Terminated",
      "event_date_terminated": "2006-07-24",
      "res_event_number": "30278",
      "product_code": "IXR",
      "k_numbers": [
        "K021491",
        "K944013",
        "K980169",
        "K991716",
        "K993645"
      ],
      "product_description": "Patient tables of CT systems with brand name: CT/e; CT/e Dual; CT/e Plus, CT/e Dual Plus; CT/e Lite; ProSpeed AI; ProSpeed AII; ProSpeed FI; ProSpeed FII; ProSpeed EII; CT HiSpeed Series.",
      "code_info": "Model or Catalog: 2297024, 2320315, 2244226, 2113694-2, 2115992-4, 2200290-2",
      "firm_fei_number": "2126677",
      "recalling_firm": "General Electric Med Systems LLC",
      "address_1": "3000 N Grandview Blvd",
      "city": "Waukesha",
      "state": "WI",
      "postal_code": "53188-1615",
      "reason_for_recall": "The patient tables of the affected CT systems are supported by a hydraulic cylinder and a cylinder shaft (i.e. the upper shaft) which connects the tabletop to the table frame.  GE received a report of a HiSpeed LX/I system table falling abruptly due to the filure of the upper shaft.  No injuries were reported.",
      "root_cause_description": "Other",
      "action": "Inadequate materials used to manufacture the upper shaft of patient tables that can result in uncontrolled table motion.",
      "product_quantity": "1150",
      "openfda": {
        "k_number": [
          "K924326",
          "K943581",
          "K883863",
          "K973039",
          "K912996",
          "K931563",
          "K965096",
          "K883153",
          "K963851",
          "K934574",
          "K792326",
          "K905153",
          "K965105",
          "K905152",
          "K953557",
          "K914417",
          "K922364",
          "K884531",
          "K896119",
          "K951176",
          "K882019",
          "K925175",
          "K901654",
          "K912586",
          "K940721",
          "K905265",
          "K883162",
          "K854478",
          "K850948",
          "K945842",
          "K874114",
          "K854486",
          "K843926",
          "K860913",
          "K896583",
          "K896324",
          "K000412",
          "K912741",
          "K840227",
          "K874113",
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          "K913147",
          "K920728",
          "K953556",
          "K905501",
          "K854085",
          "K902989",
          "K914165",
          "K760466",
          "K961022",
          "K910838",
          "K935444",
          "K853175",
          "K870707",
          "K781532",
          "K770334",
          "K792645",
          "K971128",
          "K893673",
          "K911267",
          "K950402",
          "K954356",
          "K892226",
          "K950981",
          "K920726",
          "K944987",
          "K911098",
          "K915853",
          "K840226",
          "K920742",
          "K903395",
          "K920722",
          "K922591",
          "K791812",
          "K903422",
          "K970640"
        ],
        "registration_number": [
          "3003768251",
          "9613445",
          "2529571",
          "2243057",
          "9616014",
          "8022065",
          "3009077524",
          "3008284470",
          "3013846070",
          "3015276088",
          "3004977335",
          "9610903",
          "3012010520",
          "3007912863",
          "3033527770",
          "1225473",
          "3010496070",
          "1223864",
          "3033525986",
          "3003927316",
          "8030233",
          "3000126629",
          "3002808176"
        ],
        "fei_number": [
          "3003768251",
          "2243057",
          "3002675731",
          "3009077524",
          "3008284470",
          "3013846070",
          "3015276088",
          "3004977335",
          "1000305755",
          "3012010520",
          "3007912863",
          "3033527770",
          "3001237319",
          "3002808139",
          "3010496070",
          "3003927316",
          "3033525986",
          "1000121370",
          "3002807145",
          "3003434037",
          "3000126629",
          "3002808176",
          "3002175190"
        ],
        "device_name": "Table, Radiographic, Tilting",
        "medical_specialty_description": "Radiology",
        "regulation_number": "892.1980",
        "device_class": "2"
      }
    }
  ]
}