{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Newark",
      "address_1": "500 Gbc Dr Ms 514",
      "reason_for_recall": "Siemens Healthcare Diagnostics determined that the Dimension Vista Calcium (CA) Flex reagent cartridge lot # 16060BB may produce erroneously low or high results from specific well sets.",
      "address_2": "PO BOX 6101",
      "product_quantity": "5,991 cartridges",
      "code_info": "Device Listing No: D011443  Batch Number 16060BB",
      "center_classification_date": "20161004",
      "distribution_pattern": "Distributed Nationwide and the countries of : Austria, Bahamas, Belgium, Canada, Czech Republic, Denmark, Germany, Italy, Japan, Netherlands, Portugal, Saudi Arabia, South Korea, Slovenia, and Spain.",
      "state": "DE",
      "product_description": "Dimension Vista¿ Calcium (CA) Flex¿ reagent cartridge  Device Listing No.:  D011443  Batch Number: 16060BB",
      "report_date": "20161012",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Siemens Healthcare Diagnostics, Inc.",
      "recall_number": "Z-0039-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "74987",
      "termination_date": "20170511",
      "recall_initiation_date": "20160803",
      "postal_code": "19702-2466",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}