{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Newark",
      "address_1": "500 Gbc Dr Ms 514",
      "reason_for_recall": "Customer complaints of discrepant flagged and/or un-flagged patient and QC results. Reagent probe performance may decline more quickly than anticipated and have an effect on assays with similar formulations when processed sequentially on the same reagent server.",
      "address_2": "PO BOX 6101",
      "product_quantity": "1,949",
      "code_info": "Material Nos.: 10284473, 10488224,   10444801, and 10444802",
      "center_classification_date": "20141220",
      "distribution_pattern": "Worldwide Distribution -- Austria, Australia, Belgium, Canada, Czech Republic,  Denmark, Finland, France, Germany, Italy, Japan, Malaysia,  Netherlands, New Zealand, Norway, Portugal, Republic Korea, Saudi Arabia, Slovakia, Slovenia,   South Africa, Spain, Switzerland, United Kingdom, and United States.",
      "state": "DE",
      "product_description": "Dimension Vista 500 Intelligent Lab System or Dimension Vista 1500 Intelligent Lab System:     An in vitro diagnostic device intended to duplicate manual analytical procedures such as pipetting, mixing, heating, and measuring spectral intensities to determine a variety of analytes in human body fluids.",
      "report_date": "20141231",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Siemens Healthcare Diagnostics, Inc.",
      "recall_number": "Z-0838-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "69687",
      "termination_date": "20171006",
      "more_code_info": "",
      "recall_initiation_date": "20141105",
      "postal_code": "19702-2466",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}