{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "25604",
      "product_res_number": "Z-0493-03",
      "event_date_initiated": "2002-11-27",
      "event_date_posted": "2003-01-30",
      "recall_status": "Terminated",
      "event_date_terminated": "2005-01-10",
      "res_event_number": "25329",
      "product_code": "IXR",
      "k_numbers": [
        "K923049"
      ],
      "product_description": "Uroskop D1/D2/D3 - Table, Radiographic, Stationary Top.",
      "code_info": "Uroskop D1 -- Model #9785023 Uroskop D2/D3 -- Model #9785015",
      "firm_fei_number": "2240869",
      "recalling_firm": "Siemens Medical Systems Inc",
      "address_1": "186 Wood Ave So",
      "city": "Iselin",
      "state": "NJ",
      "postal_code": "08830",
      "additional_info_contact": "Roland Richter\n732-321-4835",
      "reason_for_recall": "There is unintended system movement or unwanted automatic movement of the tabletop.",
      "root_cause_description": "Other",
      "action": "Siemens personal will install Host Software VA00F and Generator Host Software VE00D on affected Uroskop units.  Update instructions were sent to users November 27,2002 and December 7, 2002.",
      "product_quantity": "13",
      "distribution_pattern": "Product was distributed to 6 hospitals nationwide and 5 government hospitals.  Internationally, the tables were distributed to Germany, Netherlands, Italy , Luxembourg, Sweden, Austria, Switzerland, Slovakia, Hungary, Ukraine, Russia, Turkmenistan, South Africa, Canada, Malaysia, Japan, and Taiwan.",
      "openfda": {
        "k_number": [
          "K950402",
          "K912996",
          "K843926",
          "K911267",
          "K874114",
          "K771293",
          "K905152",
          "K883162",
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          "K792326",
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          "K920728",
          "K915853",
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          "K965096",
          "K874113",
          "K934574",
          "K840226",
          "K760466",
          "K945842",
          "K883863",
          "K944987",
          "K920742",
          "K965105",
          "K770334",
          "K903422",
          "K792645",
          "K896583",
          "K903395",
          "K870707",
          "K901654",
          "K940721",
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          "K953557",
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          "K850948",
          "K892226",
          "K925175",
          "K840227",
          "K971128",
          "K853175",
          "K905501",
          "K854085",
          "K910838",
          "K905265",
          "K791812",
          "K963851",
          "K911098",
          "K913147",
          "K973039",
          "K880529",
          "K882019",
          "K902989",
          "K970640",
          "K935444",
          "K884531",
          "K953556",
          "K000412",
          "K896119",
          "K950981",
          "K922591"
        ],
        "registration_number": [
          "8022065",
          "3033525986",
          "3002808176",
          "9610903",
          "3013846070",
          "3033527770",
          "3000126629",
          "1223864",
          "8030233",
          "9616014",
          "1225473",
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          "3003927316",
          "3003768251",
          "3012010520",
          "9613445",
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          "2243057",
          "2529571"
        ],
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          "3000126629",
          "3002807145",
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          "3002808139",
          "3003768251",
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          "1000305755",
          "3001237319",
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          "3002175190",
          "3010496070",
          "3004977335",
          "3015276088",
          "3008284470",
          "3009077524",
          "2243057"
        ],
        "device_name": "Table, Radiographic, Tilting",
        "medical_specialty_description": "Radiology",
        "regulation_number": "892.1980",
        "device_class": "2"
      }
    }
  ]
}