{
  "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": "74113",
      "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": "Letter",
      "distribution_pattern": "Nationwide Distribution to UT, MA, OH, IN, NC, NY, VA, CA, IA and KY.",
      "recall_number": "Z-2040-2016",
      "product_description": "Histoplasma Yeast Complement Fixation Antigen Dilute Ref# H30150  The fungal antigens and positive controls are used to detect antibodies in patient serum by the complement fixation (CF) procedure to aid in the diagnosis of four specific fungal diseases: Histoplasmosis, blastomycosis, coccidioidomycosis, and aspergillosis",
      "product_quantity": "467 units",
      "reason_for_recall": "The device was found to have bacterial contamination.",
      "recall_initiation_date": "20160509",
      "center_classification_date": "20160620",
      "termination_date": "20170110",
      "report_date": "20160629",
      "code_info": "Lot 111WH3"
    }
  ]
}