{
  "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,
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  },
  "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-2040-2023",
      "product_description": "EliA GliadinDP IgG Well in the Phadia 2500EE instrument (Material Number 12410002)  EliA GliadinDP IgG is 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\t14553901",
      "product_quantity": "568 units US",
      "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: 07333066010847 All lots",
      "more_code_info": ""
    }
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}