{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "South Burlington",
      "state": "VT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "81005",
      "recalling_firm": "Data Innovations, LLC",
      "address_1": "120 Kimball Ave Ste 100",
      "address_2": "N/A",
      "postal_code": "05403-6837",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Distributed to OK. Foreign distribution to Argentina, Hong Kong, Malaysia, Thailand, Germany, Jordan, Australia, and Switzerland.",
      "recall_number": "Z-0203-2019",
      "product_description": "IM Abbott Alinity ci-series (abdicqii) accessory driver v8.00.0001 software product that can receive information from a hospital computer system (also called a Laboratory Information System [LIS]).",
      "product_quantity": "9",
      "reason_for_recall": "Quality control results are not processed for Abbott Diagnostics Alinity ci series (abdicqii) instrument.  This has been determined to be a driver malfunction. When an instrument transmits results from a quality control (QC) sample ID  (\"Q^Control\" in SPM segment), and the option  Hold Results Until Complete  is enabled, the results do not parse into IM. The  communication Trace shows the sample being transmitted, but no information is logged in the Specimen Event Log (SEL).  There is a potential for harm if QC results are not processed, downstream auto verification rules may misfire based on missing QC  results leading to a delay in, or incorrect treatment. QC results will not be available for evaluation by the lab.  There have been no reported instances of patient harm from this malfunction.",
      "recall_initiation_date": "20180829",
      "center_classification_date": "20181022",
      "termination_date": "20190205",
      "report_date": "20181031",
      "code_info": "accessory driver version number 8.00.0001"
    }
  ]
}