{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "East Falmouth",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90820",
      "recalling_firm": "Associates of Cape Cod, Inc.",
      "address_1": "124 Bernard E Saint Jean Drive",
      "address_2": "N/A",
      "postal_code": "02536-4445",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Worldwide distribution - US Nationwide distribution in the state of CA and the countries of Austria, France, Germany, India, Ireland, Italy, Spain, UK.",
      "recall_number": "Z-1774-2022",
      "product_description": "Fungitell STAT- IVD Assay for (1 ¿ 3)-~-D-Glucan in Serum  Ref:  FT007",
      "product_quantity": "243 kits",
      "reason_for_recall": "Incorrect information on the Fungitell STAT clamshells containing the Fungitell STAT Standard, relates to printed information for reconstitution and pretreatment volumes",
      "recall_initiation_date": "20220817",
      "center_classification_date": "20220920",
      "termination_date": "20240612",
      "report_date": "20220928",
      "code_info": "UDI-DI: 00862696000227  Lot # FK22008 and Package Control # 113041 Exp. Date: 2023-11-21"
    }
  ]
}