{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Martinez",
      "address_1": "757 Arnold Dr Ste A",
      "reason_for_recall": "Siemens has become aware of a customer complaint concerning the rail threaded holes of the 550TxT treatment tabletop.  Due to a manufacturing error, the screws holding the side rails in position on the tabletop might break off.",
      "address_2": "",
      "product_quantity": "179 active devices.",
      "code_info": "ONCOR, PRIMUS and ARTISTE Lican systems with tabletop component:  Tabletop, 550TxT, TT-A    08632296*  Tabletop, 550TxT, TT-S    10046140",
      "center_classification_date": "20130826",
      "distribution_pattern": "Worldwide Distribution - USA Nationwide in the states of NJ, IN, PA, FL, OH, MN, MO, CA, AL, NE MI, LA. and countries of:Argentina, China, South Africa, Pakistan, Spain, Switzerland, Italy, Algeria, Croatia, Turkey, Canada, Germany, France, Poland, Japan, Russian Federation. Lebanon, Egypt, Slovakia, Latvia, Kenya, Brazil, Kuwait, Saudi Arabia, Greece, Belgium, Taiwan, Portugal.",
      "state": "CA",
      "product_description": "PRIMUS, ONCOR, ARTISTE Linac systems with component Tabletop, 550TxT, TT-A s/n 1001-1233 and Tabletop 550TxT, TT-S s/n 1001-1083.      Product Usage:  The intended use of the SIEMENS branded, ARTISTE\u001d, ONCOR\u001d and PRIMUS\u001d family of linear accelerator systems is to deliver X-ray photon and electron radiation for the therapeutic treatment of cancer.",
      "report_date": "20130904",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Siemens Medical Solutions USA,  Inc",
      "recall_number": "Z-2095-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "65848",
      "termination_date": "20141124",
      "more_code_info": "",
      "recall_initiation_date": "20130718",
      "postal_code": "94553-3615",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}