{
  "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,
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  },
  "results": [
    {
      "status": "Terminated",
      "city": "Tarrytown",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79683",
      "recalling_firm": "Siemens Healthcare Diagnostics, Inc.",
      "address_1": "511 Benedict Ave",
      "address_2": "N/A",
      "postal_code": "10591-5005",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "FL   and  France  Spain  Sweden  United Kingdom  Germany",
      "recall_number": "Z-1588-2018",
      "product_description": "Analyzer and Atellica IM 1600 Analyzer system for in vitro diagnostic testing of clinical specimens.",
      "product_quantity": "N/A",
      "reason_for_recall": "When more than one immunoassay analyzer is connected to a single solution system, reporting and conversion factors may not be applied to all analyzers",
      "recall_initiation_date": "20180226",
      "center_classification_date": "20180501",
      "termination_date": "20200512",
      "report_date": "20180509",
      "code_info": "UDI 00630414002026"
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}