{
  "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": "Norwood",
      "state": "MA",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "68353",
      "recalling_firm": "Siemens Healthcare Diagnostics Inc",
      "address_1": "2 Edgewater Drive",
      "address_2": "N/A",
      "postal_code": "02062",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US including the states of OR and PA., and the countries of  Denmark and UK.",
      "recall_number": "Z-2071-2014",
      "product_description": "Siemens RAPIDComm¿ Data Management System.    The RAPIDComm¿ Data Management System manages the process of sending and receiving data from Siemens POC devices and hospital systems located in the hospital network,",
      "product_quantity": "6 systems",
      "reason_for_recall": "RAPIDComm¿ 5.0 Screen Layout will display incorrect test names",
      "recall_initiation_date": "20140522",
      "center_classification_date": "20140717",
      "termination_date": "20150526",
      "report_date": "20140723",
      "code_info": "Serial Numbers: 4387, 3734, 4177, 4149, 3074, 4194"
    }
  ]
}