{
  "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": "65641",
      "product_res_number": "Z-0283-2008",
      "event_date_initiated": "2007-02-27",
      "event_date_posted": "2008-01-31",
      "recall_status": "Terminated",
      "event_date_terminated": "2011-02-03",
      "res_event_number": "45495",
      "product_code": "KPQ",
      "k_numbers": [
        "K946053"
      ],
      "product_description": "Si emans Simview NT Cassette Holder Electronic Imaging Device (Image Identifier) with CT, Part No: 54 96 984; Siemens Medical Solutions USA, Concord, CA  94520",
      "code_info": "Serial Numbers: 6013, 6003, 6078, and 6676",
      "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": "925-246-8407",
      "reason_for_recall": "Loose Mounting Screws -- Cassette holder may become  loose and result in the device dislodging and colliding with the patient.",
      "root_cause_description": "Labeling design",
      "action": "Customers were sent a Customer Safety Advisory Notice on February 27, 2007, notifying them that the mounting screws on the cassette holders on the SIMVIEW 3000 and NT Simulators, as well as some MEVASIM Simulators, could loosen and can cause damage to the system, or personal injury.  The firm requested that they check of tightness on the mounting hardware.  A STOP Modification notice was issued on 06/01/2007, to all affected regional service organizations that are responsible for implementing updates due to new information.  Updated letters and User instructions will be released in August 2007.",
      "product_quantity": "287 units total, all recalls Z-0281-285-2008",
      "distribution_pattern": "Worldwide Distribution - USA including states of IN, VA, MA, VT, NJ, NY, PA, DC, NC, SC, GA, AL, TN, MI, KY, OH, IN MI, MN, ND, MT, IL, MO, KS, NE, AR, OK, TX, AZ, CA, SD, LA, Puerto Rico, and countries of Argentina, Australia, Austria, Bangladesh, Belarus, Belgium, Brazil, Bulgaria, Canada, Colombia, Costa Rica, Croatia, Denmark, Ecuador, Egypt, El Salvador, Estonia, France, Germany, Greece, Hungary, India, Iran, Ireland, Italy, Kuwait, Lithuania, Malaysia, Mexico, Morocco, Netherlands, Norway, China, Israel/Palestine, Philippines, Poland, Portugal, Qatar, Republic of Korea, Russia, Singapore, South Africa, Spain, Thailand, Turkey, Ukraine, UK,  and Vietnam.",
      "openfda": {
        "k_number": [
          "K953233",
          "K911340",
          "K132045",
          "K971839",
          "K946053",
          "K896353",
          "K885081",
          "K884323",
          "K914926",
          "K780963",
          "K834281",
          "K812726",
          "K894568",
          "K884261",
          "K052361",
          "K913017",
          "K033339",
          "K896555",
          "K930213",
          "K033470",
          "K945838",
          "K873580",
          "K770202",
          "K851653",
          "K912466",
          "K083591",
          "K923851",
          "K032550",
          "K891293",
          "K090706",
          "K761265",
          "K782005",
          "K982857",
          "K910647",
          "K810858",
          "K946128",
          "K870221",
          "K851813",
          "K852410",
          "K850977",
          "K072445",
          "K760420",
          "K101038",
          "K910367",
          "K781496",
          "K061006",
          "K895442",
          "K921108",
          "K903313",
          "K132944",
          "K964972",
          "K951830",
          "K960737",
          "K853671",
          "K992751",
          "K022219",
          "K781519",
          "K922287",
          "K023052",
          "K921876",
          "K853349",
          "K803032",
          "K964138",
          "K021780",
          "K973848",
          "K920506",
          "K013531",
          "K052345",
          "K803124",
          "K854880"
        ],
        "registration_number": [
          "3015232217",
          "1123169",
          "1219183",
          "9617016",
          "3007545404",
          "9611343",
          "2916710"
        ],
        "fei_number": [
          "3015232217",
          "1219183",
          "3002806900",
          "1000123143",
          "1000284313",
          "3007545404",
          "2916710"
        ],
        "device_name": "System, Simulation, Radiation Therapy",
        "medical_specialty_description": "Radiology",
        "regulation_number": "892.5840",
        "device_class": "2"
      }
    }
  ]
}