{
  "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": "Irvine",
      "address_1": "34 Bunsen",
      "reason_for_recall": "Horiba Medical is recalling ABX PENTRA ML because they have confirmed an issue with the ABX PENTRA ML data management and validation system.  An incorrect patient result is transmitted to the Laboratory Information System.  This result is from a previous run of the same patient that is stored in the ML database.  This issue occurs in a very rare sequence of specific events.  The affected software",
      "address_2": "",
      "product_quantity": "10 units",
      "code_info": "Lot/Serial# PML0937",
      "center_classification_date": "20130107",
      "distribution_pattern": "Nationwide in the US, including the states of CA, MI, IN, FL, and GA. Center Recall Depth is Retail.",
      "state": "CA",
      "product_description": "ABX PENTRA ML, Software Versions: V8.0.x and Below; V.9.0.1 and V9.0.2",
      "report_date": "20130116",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Horiba Instruments, Inc dba Horiba Medical",
      "recall_number": "Z-0645-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "63829",
      "termination_date": "20130312",
      "more_code_info": "",
      "recall_initiation_date": "20120920",
      "postal_code": "92618-4210",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}