{
  "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": "Terminated",
      "city": "Indianapolis",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84260",
      "recalling_firm": "Roche Diagnostics Operations, Inc.",
      "address_1": "9115 Hague Rd",
      "address_2": "N/A",
      "postal_code": "46256-1025",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-0669-2020",
      "product_description": "Elecsys Anti-HAV IgM assay-for the in vitro qualitative detection of IgM antibodies to hepatitis A virus (anti-HAV IgM) in human serum and plasma   Catalog number:  07026773190",
      "product_quantity": "712 units",
      "reason_for_recall": "Current  software version of the Anti-HAV IgM APP-file (version 06.05-101) downloaded  an erroneous Border Area setting, (1.0   1.00) instead of (0.90   1.10).",
      "recall_initiation_date": "20191028",
      "center_classification_date": "20191212",
      "termination_date": "20220628",
      "report_date": "20191218",
      "code_info": "Anti-HAV IgM APP-file (version 06.05-101)",
      "more_code_info": ""
    }
  ]
}