{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Newark",
      "address_1": "500 Gbc Dr Ms 514",
      "reason_for_recall": "Siemens Healthcare Diagnostics has determined that the sample query function that includes \u001cInstrument\u001d or \u001cInstrument Group\u001d as search criteria may not return all samples from the Dimension Vista systems if onboard aliquot support rules are configured in the CentraLink system.",
      "address_2": "PO BOX 6101",
      "product_quantity": "1941",
      "code_info": "Product: Siemens CentraLink Data Management System, v14.0.5  Material Number (SMN)10811741, 10811742, 10811743, 10814298, 10814877, 10814880,10814881,     Product: CentraLink Data Management System, v14.0.8  Material Number (SMN)10815474, 10816519, 10816520, 10816521, 10816522, 10816523, 10816524, 10817180, 10817181",
      "center_classification_date": "20150702",
      "distribution_pattern": "Worldwide Distribution - Nationwide Distribution and to the countries of : Belgium, Canada, Czech Republic, Denmark, France, Germany, Italy, Netherlands, Saudi Arabia, Spain, Switzerland and United Kingdom.",
      "state": "DE",
      "product_description": "CentraLink\" Data Management System; software is a network solution provider and multi-system data manager for the instruments and lab automation systems (LAS) within the lab. The CentraLink software consolidates data  from all connected instruments so that an operator can review and edit patient and quality control results from a single location.",
      "report_date": "20150708",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Siemens Healthcare Diagnostics, Inc.",
      "recall_number": "Z-1957-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "71362",
      "termination_date": "20180427",
      "more_code_info": "",
      "recall_initiation_date": "20150519",
      "postal_code": "19702-2466",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}