{
  "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": "62989",
      "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": "US Nationwide Distribution including the states of: GA, IA, KS, NC and TX.",
      "recall_number": "Z-2367-2012",
      "product_description": "Siemens Mobilett Mira mobile x-ray system      Product Usage:  Mobile x-ray system",
      "product_quantity": "9",
      "reason_for_recall": "During regular product monitoring, firm became aware of a potential issue with the Mobilett Mira system, (serial numbers 1034, 1038, 1041, 1042, 1043, 1050, 1053, and 1054.  During normal clinical operation the center screw on the driving wheel may become loose resulting in system immobilization.  There is no risk of the system tipping over or collapsing on the floor, however the system may tilt t",
      "recall_initiation_date": "20120430",
      "center_classification_date": "20120911",
      "termination_date": "20120925",
      "report_date": "20120919",
      "code_info": "Model number 10273100 - serial numbers 1034, 1038, 1041, 1042, 1043, 1050, 1053, and 1054"
    }
  ]
}