{
  "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": "Ann Arbor",
      "state": "MI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "62581",
      "recalling_firm": "Siemens Medical Solutions, USA, Inc",
      "address_1": "400 Morgan Rd",
      "address_2": "N/A",
      "postal_code": "48108",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution -- MA, GA, MO, IA, CA, PA, OR, CO, NY, NJ, WA, UT, OH, WI, MI, KY, and NC.",
      "recall_number": "Z-2219-2012",
      "product_description": "syngo Dynamics Version 9.5",
      "product_quantity": "30",
      "reason_for_recall": "If multiple uncompressed images/clips are sent to the syngo Dynamics server, around the same time, it is possible for an image from a patient to be placed in another patient's study.",
      "recall_initiation_date": "20120713",
      "center_classification_date": "20120817",
      "termination_date": "20130715",
      "report_date": "20120829",
      "code_info": "10091862 and 10091863"
    }
  ]
}