{
  "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": [
    {
      "status": "Terminated",
      "city": "Athens",
      "state": "OH",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79642",
      "recalling_firm": "Diagnostic Hybrids, Inc.",
      "address_1": "2005 E State St Ste 100",
      "address_2": "N/A",
      "postal_code": "45701-2125",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) to the states of :  CO, CT, IA, IL, MN, MO, NC, NY, OH TX, and UT., and to the countries of : Switzerland, India, Hong Kong, and Japan.",
      "recall_number": "Z-1499-2018",
      "product_description": "MicroVue SC5b-9 Plus EIA (CE-IVD), Model A029.  An enzyme immunoassay for the quantitation of SC5b-9 complex present in human plasma or serum.",
      "product_quantity": "72 kits",
      "reason_for_recall": "A component of the kit was found to contain bacterial contamination.",
      "recall_initiation_date": "20151103",
      "center_classification_date": "20180424",
      "termination_date": "20200828",
      "report_date": "20180502",
      "code_info": "Lot 052419"
    }
  ]
}