{
  "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": "2026-04-01",
    "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": "85368",
      "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": "Worldwide distribution - US Nationwide distribution including in the states of AZ, CA, FL, IL, IN,  MI, MN, NY,TX, UT, VA, WI and the countries of France, Spain, Hong Kong, United Kingdom.",
      "recall_number": "Z-2301-2020",
      "product_description": "Histoplasma Immunodiffusion (ID) Antigen; The IFU labeling is for multiple products which included Fungal Antigens, Positive Controls and ID Plates,and Immunodiffusion (ID) Plates for use in the ID Test, Histoplasma ID Antigen",
      "product_quantity": "155 vials",
      "reason_for_recall": "False positive results due to potential contamination of reagent.",
      "recall_initiation_date": "20191104",
      "center_classification_date": "20200609",
      "termination_date": "20220527",
      "report_date": "20200617",
      "code_info": "Lot number L106909; UDI # (01) 00816387020391 (17) 220610(10)L106909"
    }
  ]
}