{
  "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,
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  },
  "results": [
    {
      "country": "United States",
      "city": "Newark",
      "address_1": "500 Gbc Dr Ms 514",
      "reason_for_recall": "Certain configuration parameters may cause the reference ranges to not hold results as expected and release them to the Laboratory Information System (LIS) that should have been held for manual review.",
      "address_2": "PO BOX 6101",
      "product_quantity": "336",
      "code_info": "syngo Lab Data Manager Application Software versions VA11B, VA12A, and VA12B",
      "center_classification_date": "20140630",
      "distribution_pattern": "Worldwide Distribution.  US Nationwide, Canada, Australia, Belgium, Czech Republic, Germany, Denmark, Finland, France, United Kingdom, Italy, Netherlands, Portugal, Slovakia, Singapore, Japan, and Spain.",
      "state": "DE",
      "product_description": "syngo Lab Data Manager, SMN 10800057, 10803189, and 10804573.",
      "report_date": "20140709",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Siemens Healthcare Diagnostics, Inc.",
      "recall_number": "Z-1944-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "68394",
      "termination_date": "20150810",
      "more_code_info": "",
      "recall_initiation_date": "20140520",
      "postal_code": "19702-2466",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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}