{
  "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": "Malvern",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "62988",
      "recalling_firm": "Siemens Medical Solutions USA, Inc",
      "address_1": "51 Valley Stream Pkwy",
      "address_2": "N/A",
      "postal_code": "19355",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide distribution: USA including states of:  IN, MI, MS, TN and TX.",
      "recall_number": "Z-2341-2012",
      "product_description": "Siemens Uroskop Access.    Fluoroscopic, image intensified x-ray system",
      "product_quantity": "5",
      "reason_for_recall": "Siemens has discovered a possible hazard to patients or hospital personnel when tilting the Uroskop Access system starting with serial number 6076.  When tilting the table on the Uroskop Access table, the motor may become disconnected and the entire table assembly may fall on the floor.",
      "recall_initiation_date": "20120430",
      "center_classification_date": "20120910",
      "termination_date": "20120920",
      "report_date": "20120919",
      "code_info": "Model number 5756130 -- serial numbers 6076, 6078, 6080, 6081, and 6082."
    }
  ]
}