{
  "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": "Dimension Vista Myoglobin Calibrator (MYO CAL) may produce a positive shift in MYO QC and Patient test results that exceeds acceptance criteria for this product. A positive shift observed up to 12% at MYO concentrations within and above the reference range of the assay. Depending on quality control limits, this drift may not be detected.",
      "address_2": "PO BOX 6101",
      "product_quantity": "1230",
      "code_info": "Lot 4FD085, exp. 12-01-2014",
      "center_classification_date": "20150108",
      "distribution_pattern": "Worldwide Distribution: US (nationwide) and country of: Canada.",
      "state": "DE",
      "product_description": "Dimension Vista Myoglobin Calibrator (MYO CAL), Lot 4FD085     Product usage: in vitro diagnostic product for the calibration of Myoglobin (MYO) method on the Dimension Vista System.",
      "report_date": "20150114",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Siemens Healthcare Diagnostics, Inc.",
      "recall_number": "Z-0946-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "69937",
      "termination_date": "20161213",
      "more_code_info": "",
      "recall_initiation_date": "20141124",
      "postal_code": "19702-2466",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}