{
  "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": "Norman",
      "state": "OK",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76159",
      "recalling_firm": "Immuno-Mycologics, Inc",
      "address_1": "2700 Technology Pl",
      "address_2": "N/A",
      "postal_code": "73071-1127",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Nationwide throughout the US",
      "recall_number": "Z-1109-2017",
      "product_description": "Cryptococcal Antigen Lateral Flow Assay (CrAg LFA), Reference # CR2003",
      "product_quantity": "630 units",
      "reason_for_recall": "The affected products have approximately a 91% specificity while the non-affected lots have approximately a 99% specificity. The recalling firm is aware of three customers who reported false positive results.",
      "recall_initiation_date": "20161227",
      "center_classification_date": "20170127",
      "termination_date": "20170308",
      "report_date": "20170208",
      "code_info": "161028133653JH, 161003111544KH, and 161007105036JG",
      "more_code_info": ""
    }
  ]
}