{
  "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": [
    {
      "status": "Terminated",
      "city": "Mountain View",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "70361",
      "recalling_firm": "Siemens Medical Solutions USA, Inc.",
      "address_1": "685 E Middlefield Rd",
      "address_2": "N/A",
      "postal_code": "94043-4045",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution -- US, including the states of TX and MN, and the territory of P.R.; and, the countries of China, Germany, Russian Fed, Saudi Arabia, Taiwan, France, Thailand, and Italy.",
      "recall_number": "Z-1063-2015",
      "product_description": "ACUSON S2000 Automated Breast Volume Scanner (ABVS), model number 10434730.  The affected sub-components are #10434968 - Boom Welding and 10434969 - Arm Welding.    The S2000 ABVS ultrasound System for imaging the breast allows volumetric acquisition of the breast image.",
      "product_quantity": "24 units",
      "reason_for_recall": "There is a low probability the scanner arm will become completely detached from the scanner column.",
      "recall_initiation_date": "20150112",
      "center_classification_date": "20150207",
      "termination_date": "20150610",
      "report_date": "20150218",
      "code_info": "Serial numbers 250157-250190."
    }
  ]
}