{
  "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,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Uppsala",
      "state": "N/A",
      "country": "Sweden",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82979",
      "recalling_firm": "Phadia Ab",
      "address_1": "Rapsgatan Plant",
      "address_2": "Rapsgatan 7",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide n the states of NJ, NY, MI, WV, TX  including  PR",
      "recall_number": "Z-1907-2019",
      "product_description": "EliA RF IgM Well, REF 14-5600-01    Product Usage:  Usage:  EliA RF IgM is intended for the in vitro quantitative measurement of IgM class rheumatoid factor antibodies in human serum and plasma (Li-heparin and EDTA) to aid in the diagnosis of rheumatoid arthritis in conjunction with other laboratory and clinical findings. EliA RF IgM uses the EliA IgM method on the instrument Phadia 100, Phadia 250, Phadia 2500 and Phadia 5000.",
      "product_quantity": "30 kits",
      "reason_for_recall": "Potential for reporting low assay results",
      "recall_initiation_date": "20190510",
      "center_classification_date": "20190701",
      "termination_date": "20200602",
      "report_date": "20190710",
      "code_info": "UDI (01) 07333066010854 (17) 200630 (10) 0085  Lot Number - 0085"
    }
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}