{
  "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": "86970",
      "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, Bahrain,   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, Vatika City, Vietnam.",
      "recall_number": "Z-0863-2021",
      "product_description": "Atellica IM 1600 Analyzer - In vitro diagnostic testing of clinical specimens. Product Siemens Material Number (SMN): 11066000 - Product Usage: intended for the qualitative and quantitative analysis of various body fluids, using photometric, turbidimetric, chemiluminescent, and integrated ion selective electrode technology for clinical use.",
      "product_quantity": "1588 units",
      "reason_for_recall": "Multiple issues in Software v1.23.2 and lower-may lead to the reporting of discrepant patient results",
      "recall_initiation_date": "20201202",
      "center_classification_date": "20210114",
      "termination_date": "20240606",
      "report_date": "20210120",
      "code_info": "Software (SW) versions V1.23.2 (SMN 11469032) or lower"
    }
  ]
}