{
  "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": "Athens",
      "address_1": "1055 E State St",
      "reason_for_recall": "Samples are quantitating incorrectly, with approximately 50% higher concentration values than previously reported and historically documented.",
      "address_2": "Suite 100",
      "product_quantity": "171",
      "code_info": "Model Number A027; Lot Number 018186;   (self-affixed, EDMA Code: 12 01 02 04 00; Complement Component Bb)",
      "center_classification_date": "20150903",
      "distribution_pattern": "Worldwide Distribution - USA, including AL, CO, CT, FL, KY, MN, NC, NV, OH, PA, and WA; and, the countries of Canada, China, India, and Switzerland.",
      "state": "OH",
      "product_description": "MicroVue Bb Plus EIA is packaged as a kit which contains all reagent components to perform the test.  In vitro diagnostic.",
      "report_date": "20150909",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Diagnostic Hybrids Inc",
      "recall_number": "Z-0417-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "69545",
      "termination_date": "20150903",
      "recall_initiation_date": "20141016",
      "postal_code": "45701-7911",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}