{
  "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": "Ongoing",
      "city": "East Brisbane",
      "state": "N/A",
      "country": "Australia",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88801",
      "recalling_firm": "ELLUME LTD",
      "address_1": "57 Didsbury St",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "U.S.: MN, NY, PA, RI, UT, WA.    O.U.S.: Not provided",
      "recall_number": "Z-0183-2022",
      "product_description": "Ellume COVID-19 Home Test",
      "product_quantity": "427,994 kits",
      "reason_for_recall": "Due to a higher rate of false positive test results.",
      "recall_initiation_date": "20211001",
      "center_classification_date": "20211110",
      "report_date": "20211117",
      "code_info": "Catalogue number I-SRS-C-01  Master Lot Numbers:  21047-4;  21047-5;  21089-1;  21117-1;  PF06Z-H;  21099-1;  21124-1;  21125-1;  PF03X-H;  PF057-H;  PF05W-H;  PF069-H;  PF06E-H;  PF06N-H;  PF06Z-H;  PG080-H;  PG08H-H;  PH08X-H;",
      "more_code_info": ""
    }
  ]
}