{
  "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": {
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  "results": [
    {
      "country": "United States",
      "city": "Tarrytown",
      "address_1": "511 Benedict Ave",
      "reason_for_recall": "Siemens Healthcare Diagnostics issued a Urgent Medical Device Correction due to Ration Parameters Flagging Behavior for All Software Versions utilized on ADVIA 1200, 1650, 1800 or 2400 Chemistry Systems.",
      "address_2": "",
      "product_quantity": "876 units",
      "code_info": "Product Code: 10639265",
      "center_classification_date": "20131118",
      "distribution_pattern": "Worldwide Distribution-USA (nationwide) and the countries of  Sweden, Switzerland, Taiwan, Turkey, United Kingdom, and Vietnam.",
      "state": "NY",
      "product_description": "ADVIA 2400 System Software V4.01.    Performs assays for general and specialty chemistries, methods for specific protein measurement, drugs-of-abuse testing and therapeutic drug monitoring.",
      "report_date": "20131127",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Siemens Healthcare Diagnostics",
      "recall_number": "Z-0346-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "66069",
      "termination_date": "20170307",
      "more_code_info": "",
      "recall_initiation_date": "20130903",
      "postal_code": "10591-5005",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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}