{
  "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": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Newark",
      "address_1": "500 Gbc Dr Ms 514",
      "reason_for_recall": "An overflow flag //// is displayed in the result column for a test when the algorithm for the test cannot calculate a result or when the concentration cannot be determined because it is outside the absorbance limits, and it is possible for the user to misinterpret or edit the result.",
      "address_2": "PO BOX 6101",
      "product_quantity": "1563",
      "code_info": "ADVIA 1200 with software versions: V2.00 and V2.01    ADVIA 1650 with software versions V3.52 and V4.01",
      "center_classification_date": "20140121",
      "distribution_pattern": "Worldwide Distribution.  USA nationwide and the country of Canada.",
      "state": "DE",
      "product_description": "Siemens ADVIA 1200 and ADVIA 1650 Chemistry Systems.    Automated, clinical chemistry analyzers that can run tests on human serum, plasma, or urine.",
      "report_date": "20140129",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Siemens Healthcare Diagnostics, Inc.",
      "recall_number": "Z-0800-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "67030",
      "termination_date": "20140826",
      "more_code_info": "",
      "recall_initiation_date": "20131217",
      "postal_code": "19702-2466",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}