{
  "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": [
    {
      "status": "Terminated",
      "city": "Bethlehem",
      "state": "PA",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "74843",
      "recalling_firm": "OraSure Technologies, Inc.",
      "address_1": "1745 Eaton Ave",
      "address_2": "N/A",
      "postal_code": "18018-1769",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Distributed to one customer only in US state of Georgia.",
      "recall_number": "Z-2403-2016",
      "product_description": "OraQuick Ebola Rapid Antigen Test, Product Code  3001-2807;   Intended for the qualitative detection of antigens for Ebola viruses.",
      "product_quantity": "3,075 units",
      "reason_for_recall": "Failed stability testing at 8 months.  This lot produced intermittent false negative results for the positive kit control with devices stored at 30C conditions.",
      "recall_initiation_date": "20160720",
      "center_classification_date": "20160817",
      "termination_date": "20170510",
      "report_date": "20160824",
      "code_info": "Product Code  3001-2807 and the lot number is 6648965. Expiration date October 31, 2016."
    }
  ]
}