{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Norman",
      "state": "OK",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "96315",
      "recalling_firm": "Immuno-Mycologics, Inc",
      "address_1": "2701 Corporate Centre Dr",
      "address_2": "N/A",
      "postal_code": "73069-2901",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide - US Nationwide distribution in the states of CA and OK and the countries of Peru France, Austria, Venezuela.",
      "recall_number": "Z-1389-2025",
      "product_description": "Candida ID Antigen, REAG, AG, REF C50110, Vol 1 mL    REF ID1001, Immy Fungal Antigens, Positive Controls, & Immunodiffusion (ID) plates for use in the ID test, RX only, IVD, CE",
      "product_quantity": "30 vials",
      "reason_for_recall": "Candida Immunodiffusion Antigen may have reduced sensitivity which could result in false negative results.",
      "recall_initiation_date": "20250210",
      "center_classification_date": "20250318",
      "report_date": "20250326",
      "code_info": "Lot #: F4171005/UDI: 00816387020223"
    }
  ]
}