{
  "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": "86718",
      "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": "Worldwide distribution - US Nationwide distribution and the countries of Algeria, Argentina, Australia, Austria, Bangladesh,   Belgium, Brazil, Bulgaria, Canada, Chile, Colombia, Croatia,   Cura¿ao, Cyprus, Czech Republic, Denmark, Dominican Republic, Ecuador, Egypt, Estonia, Finland, France, Germany,   Greece, Hungary, India, Indonesia, Iran, Iraq, Ireland, Israel,   Italy, Japan, Jordan, Kenya, Kuwait, Latvia, Libya, Lithuania,   Malaysia, Mexico, Netherlands, New Zealand, Norway, Oman,   P.R. China, Pakistan, Peru, Poland, Portugal, Qatar Republic, Korea, Romania, Russian Fed., Saudi Arabia, Singapore,   Slovakia, Slovenia, South Africa, Spain, Sweden, Switzerland,   Taiwan, Thailand, Turkey, U.A.E., Ukraine, United Kingdom,  Uruguay, Vatikancity, Vietnam.",
      "recall_number": "Z-0473-2021",
      "product_description": "Atellica IM 1300 Analyzer - Product Usage: automated, immunoassay analyzers designed to perform in vitro diagnostic tests on clinical specimens. Siemens Material Number (SMN): 11066001",
      "product_quantity": "US 392 units;\tOUS 449 units",
      "reason_for_recall": "Test Definition scanning may reset custom settings to defaults causing falsely low or high results. When a 2D Master Curve and TDef barcode for a new kit lot of reagent is scanned and the TDef version is a newer version than the version that is currently on the system, some of the customer defined settings for that assay may reset to default values",
      "recall_initiation_date": "20201026",
      "center_classification_date": "20201119",
      "termination_date": "20240419",
      "report_date": "20201125",
      "code_info": "Software version: V1.23.1 or lower  UDI:  00630414007960"
    }
  ]
}