{
  "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": "Lincoln",
      "address_1": "27 Wellington Rd",
      "reason_for_recall": "High positive calcium bias on plasma sample versus results on serum",
      "address_2": "",
      "product_quantity": "213 units",
      "code_info": "All lots",
      "center_classification_date": "20140114",
      "distribution_pattern": "Nationwide Distribution",
      "state": "RI",
      "product_description": "Consult Diagnostics¿ Eon Calcium Reagent For In-Vitro Diagnostic Use  PN: 1429  For the quantitative measurement of calcium in plasma and serum",
      "report_date": "20140122",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Vital Diagnostics, Inc.",
      "recall_number": "Z-0733-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "66202",
      "termination_date": "20150826",
      "more_code_info": "",
      "recall_initiation_date": "20130829",
      "postal_code": "02865-4411",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}