{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Redmond",
      "state": "WA",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "66293",
      "recalling_firm": "Bio-Rad Laboratories",
      "address_1": "6565 185th Ave NE",
      "address_2": "N/A",
      "postal_code": "98052-5039",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution including the states of  FL, IA, ME, MO, MS, NE, NY, TN, TX, and WA",
      "recall_number": "Z-0032-2014",
      "product_description": "FSE Image Upgrade Kit, Catalog # 92019C    This kit is used to install and/or upgrade software used with the EVOLIS Microplate System.",
      "product_quantity": "23 kits",
      "reason_for_recall": "The FSE Image Upgrade kit (part 92019C) is recalled due to issue related to the export of data from the EVOLIS analyzer to Laboratory Information Systems (LIS) when using the MONOLISA Anti-HBs EIA  Quantitative Determination in EVOLIS APF version 6.0.",
      "recall_initiation_date": "20130820",
      "center_classification_date": "20131021",
      "termination_date": "20131113",
      "report_date": "20131030",
      "code_info": "Lot 122822"
    }
  ]
}