{
  "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,
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  },
  "results": [
    {
      "country": "United States",
      "city": "Irvine",
      "address_1": "34 Bunsen",
      "reason_for_recall": "Horiba Medical is recalling the ABX PENTRA N Control because it has been updated to include a revised Target Value assignment for Potassium.",
      "address_2": "",
      "product_quantity": "698 units total (80 units in US)",
      "code_info": "Lot No. 1300801",
      "center_classification_date": "20140131",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide)",
      "state": "CA",
      "product_description": "ABX PENTRA N Control, Model No. A11A01653    The ABX PENTRA N Control is for use in quality control by monitoring accuracy and precision for the quantitative methods as specified in the enclosed annex.",
      "report_date": "20140212",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Horiba Instruments, Inc dba Horiba Medical",
      "recall_number": "Z-0904-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "66912",
      "termination_date": "20141028",
      "more_code_info": "",
      "recall_initiation_date": "20131121",
      "postal_code": "92618-4210",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}