{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Newark",
      "address_1": "500 Gbc Dr Ms 514",
      "reason_for_recall": "May produce erroneously low results from specific well sets.",
      "address_2": "Po Box 6101",
      "product_quantity": "6000",
      "code_info": "Lot # 17171BD, UDI # (UDI) 0084276801561817171BD18062010445160  EXP. 06-20-2018",
      "center_classification_date": "20180427",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) and to the following countries:  Australia,  Austria,  Belgium,  Canada,  Czech Republic,  Denmark,  France,  Germany,  Italy,  Japan,  Norway,  Portugal,  Slovakia,  Slovenia,  South Korea,  Spain,  Switzerland",
      "state": "DE",
      "product_description": "Dimension Vista¿ Calcium Flex¿ reagent cartridge, Dimension Vista¿ CA, K1023, SMN # 10445160    The CA method is an in vitro diagnostic test for the quantitative measurement of calcium in human serum, plasma, and urine on the Dimension Vista System.",
      "report_date": "20180509",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Siemens Healthcare Diagnostics, Inc.",
      "recall_number": "Z-1540-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "79593",
      "termination_date": "20190516",
      "recall_initiation_date": "20180130",
      "postal_code": "19702-2466",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}