{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Irvine",
      "address_1": "34 Bunsen",
      "reason_for_recall": "The ABX PENTRA Reagent Containers do not always sit properly into the reagent rack.  In low reagent level scenarios, this could lead to insufficient reagent volume being pipetted and could lead to incorrect results being reported without an alarm.",
      "address_2": "",
      "product_quantity": "10 bags, 100 units each",
      "code_info": "DATE - MVT 25.08.2017",
      "center_classification_date": "20180131",
      "distribution_pattern": "Nationwide",
      "state": "CA",
      "product_description": "10 ML REAGENT CUP, B1034626, SAP 1221034626 for use with ABX PENTRA 400 / PENTRA C400",
      "report_date": "20180207",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Horiba Instruments, Inc dba Horiba Medical",
      "recall_number": "Z-0493-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "78692",
      "termination_date": "20191104",
      "more_code_info": "",
      "recall_initiation_date": "20171121",
      "postal_code": "92618-4210",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}