{
  "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": "Irvine",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "67528",
      "recalling_firm": "Horiba Instruments, Inc dba Horiba Medical",
      "address_1": "34 Bunsen",
      "address_2": "N/A",
      "postal_code": "92618-4210",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "USA Nationwide Distribution",
      "recall_number": "Z-1173-2014",
      "product_description": "Device Name: ABX PENTRA ML  Model/Part #(s): A11A01652  Lot/Serial #(s): N/A  Software Version(s): All versions are subject to this correction.      Product Usage:  The ABX PENTRA ML is a software data management system intended for use on ABX Hematology Analyzers.",
      "product_quantity": "15",
      "reason_for_recall": "HORIBA Medical initiated this recall of all software versions of ABX PENTRA ML (Model A11A06152) due to a software bug with the potential of transmitting incorrect results to the Laboratory Information System.",
      "recall_initiation_date": "20140214",
      "center_classification_date": "20140310",
      "termination_date": "20140822",
      "report_date": "20140319",
      "code_info": "Model/Part #(s): A11A01652  Lot/Serial #(s): N/A  Software Version(s): All versions are subject to this correction.  Shelf Life: N/A"
    }
  ]
}