{
  "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": "Ongoing",
      "city": "Portage",
      "state": "MI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92365",
      "recalling_firm": "Phadia US Inc",
      "address_1": "4169 Commercial Ave",
      "address_2": "N/A",
      "postal_code": "49002-9701",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US: CA, NJ, MI",
      "recall_number": "Z-2041-2023",
      "product_description": "Phadia 2500EE instrument -Intended for the in vitro semi-quantitative measurement of IgG antibodies directed to gliadin in human serum or plasma (Li-heparin, EDTA) to aid in the diagnosis of celiac disease  Material Number 12410002",
      "product_quantity": "9 units",
      "reason_for_recall": "Higher reported results when running EliA GliadinDP IgG Well on the instruments Phadia 2500EE compared to running EliA GliadinDP IgG Well on Phadia 250 instrument",
      "recall_initiation_date": "20230501",
      "center_classification_date": "20230629",
      "report_date": "20230705",
      "code_info": "UDI: 07333066020938 All Serial Numbers",
      "more_code_info": ""
    }
  ]
}