{
  "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,
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    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Newark",
      "address_1": "500 Gbc Dr Ms 514",
      "reason_for_recall": "Siemens Healthcare Diagnostics has become aware of deferoxamine interference with Dimension and Dimension Vista IRON assays at a different concentration than listed in the Instructions for Use (IFU).",
      "address_2": "PO BOX 6101",
      "product_quantity": "30,247 units",
      "code_info": "Device Listing # D011391  Lot # 15244AB, 15301BA,15345BB,16026BA,16075BB,16117BD,16166BA,16201BD  Exp Date 08-31-2016 - 07/19-2016.",
      "center_classification_date": "20161111",
      "distribution_pattern": "Distributed Nationwide",
      "state": "DE",
      "product_description": "Dimension Vista IRON Flex reagent cartridges",
      "report_date": "20161123",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Siemens Healthcare Diagnostics, Inc.",
      "recall_number": "Z-0401-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "75256",
      "termination_date": "20171201",
      "recall_initiation_date": "20160825",
      "postal_code": "19702-2466",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}