{
  "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,
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  "results": [
    {
      "country": "United States",
      "city": "Newark",
      "address_1": "500 Gbc Dr Ms 514",
      "reason_for_recall": "Through investigation of customer complaints, Siemens Healthcare Diagnostics has confirmed an increase in System Check failures due to high System Check LOCI results. Upon further investigation, Siemens has determined that many of these errors are due to the current limit set for System Check LOCI results.  The errors have no impact on results, but they may cause customer inconvenience.  Siemens h",
      "address_2": "PO BOX 6101",
      "product_quantity": "2207 total",
      "code_info": "Siemens Material Number 10486890",
      "center_classification_date": "20130401",
      "distribution_pattern": "Worldwide Distribution.",
      "state": "DE",
      "product_description": "Siemens Dimension(R) EXL(TM) LM (Siemens Material Number 10486890).    Intended to measure a variety of analytes in human body fluids.",
      "report_date": "20130410",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Siemens Healthcare Diagnostics, Inc.",
      "recall_number": "Z-1046-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "64570",
      "termination_date": "20140114",
      "recall_initiation_date": "20130227",
      "postal_code": "19702-2466",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}