{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Tarrytown",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83655",
      "recalling_firm": "Siemens Healthcare Diagnostics, Inc.",
      "address_1": "511 Benedict Ave",
      "address_2": "",
      "postal_code": "10591-5005",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide  Foreign:  Argentina  Australia  Bangladesh  Belgium  Brazil  Colombia  Dominican Republic  Finland  France  Germany  Greece  Italy  Japan  Latvia  Mexico  Netherlands  P.R. China  Republic Korea  Singapore  Spain  Switzerland  Thailand  United Kingdom  Vietnam",
      "recall_number": "Z-0205-2020",
      "product_description": "Atellica IM  1600 Analyzer, (SW) version V1.19.0 and V1.19.2  Siemens Material Number (SMN): 11066000",
      "product_quantity": "166 total  US: 15; OUS:151",
      "reason_for_recall": "Issues Scanning New Reagent Lot Test Definition on the  Atellica IM 1300 Analyzer and Atellica IM 1600 Analyzer  SW V 1.19.0 and 1.19.2",
      "recall_initiation_date": "20190815",
      "center_classification_date": "20191024",
      "termination_date": "20220505",
      "report_date": "20191030",
      "code_info": "(SW) version V1.19.0 and V1.19.2  UDI:  00630414002026",
      "more_code_info": ""
    }
  ]
}