{
  "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": "Ongoing",
      "city": "South Australia",
      "state": "",
      "country": "Australia",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98539",
      "recalling_firm": "Oxoid Australia Pty Limited",
      "address_1": "20 Dlgleish St",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of GA and CA.",
      "recall_number": "Z-1766-2026",
      "product_description": "OXOID MICROBACT IDENTIFICATION KITS, Listeria 12L Kit, 20 Tests; Listeria identification sysystem",
      "product_quantity": "2 kits",
      "reason_for_recall": "Oxoid Ltd., part of Thermo Fisher Scientific, confirmed that Microbact 12L Kit 20 Tests MB1128A lot 4494873  may identify incorrect organism due to inconclusive result from ambiguous color reactions in wells.",
      "recall_initiation_date": "20260303",
      "center_classification_date": "20260402",
      "report_date": "20260408",
      "code_info": "UDI/DI 5032384127498, Lot Number 4494873",
      "more_code_info": ""
    }
  ]
}