{
  "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": "395 units",
      "code_info": "All lots",
      "center_classification_date": "20140114",
      "distribution_pattern": "Nationwide Distribution",
      "state": "RI",
      "product_description": "Vital Diagnostics Envoy Calcium Reagent For In-Vitro Diagnostic Use.  PN 55285  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-0732-2014",
      "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"
    }
  ]
}