{
  "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": [
    {
      "country": "United States",
      "city": "Brea",
      "address_1": "250 S Kraemer Blvd",
      "reason_for_recall": "Beckman Coulter is recalling the Access 2 Immunoassay System because they determined that the fuses in the system may be of the wrong amperage.",
      "address_2": "",
      "product_quantity": "8 units total (1 unit in the US)",
      "code_info": "Serial Numbers:   508801, 508802, 508803, 508804, 508805, 508806, 508807, 508810",
      "center_classification_date": "20131114",
      "distribution_pattern": "Worldwide distribution: US (nationwide) in the state of: TX and countries of: Colombia, Hong Kong and Korea.",
      "state": "CA",
      "product_description": "Access 2 Immunoassay System, Part Number: 81600N    The Access Immunoassay System is an in vitro diagnostic device used for the quantitative, semi-quantitative or qualitative determination of various analyte concentrations found in human body fluids.",
      "report_date": "20131120",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Beckman Coulter Inc.",
      "recall_number": "Z-0291-2014",
      "initial_firm_notification": "Telephone",
      "product_type": "Devices",
      "event_id": "66397",
      "termination_date": "20131114",
      "more_code_info": "",
      "recall_initiation_date": "20130912",
      "postal_code": "92821-6232",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}