{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Newark",
      "address_1": "500 Gbc Dr Ms 514",
      "reason_for_recall": "Imprecision with certain lots",
      "address_2": "PO BOX 6101",
      "product_quantity": "4963",
      "code_info": "Lots: E5-E7, F1-F5, 1290, 1300, 1313, 1330, 1338, 1367, 1371, and 1380.",
      "center_classification_date": "20131107",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) and Mexico.",
      "state": "DE",
      "product_description": "Emit 2000 Phenobarbital Assay and Syva Emit 2000 Phenobarbital Assay",
      "report_date": "20131113",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Siemens Healthcare Diagnostics, Inc.",
      "recall_number": "Z-0181-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "66267",
      "termination_date": "20140827",
      "recall_initiation_date": "20130830",
      "postal_code": "19702-2466",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}