{
  "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": "2026-08-12",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Munchen",
      "state": "",
      "country": "Germany",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98927",
      "recalling_firm": "Beckman Coulter Biomedical GmbH",
      "address_1": "Sauerbruchstr. 50",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S.: FL, GA, IL, MI, and PA  O.U.S.: Belgium, France, Hungary, Poland, Taiwan (Province of China), Tunisia, United Arab Emirates, and United Kingdom of Great Britain and Northern Ireland.",
      "recall_number": "Z-2834-2026",
      "product_description": "REMISOL Advance with Software Version 2.5  UDI-DI code: 15099590802073    The Normand Info REMISOL Advance Data Manager collects and manages data and workflow for 128 connections",
      "product_quantity": "20 systems",
      "reason_for_recall": "Due to software issues where does not handle combo assay results.  The software may replace the final combo test result with one of the sub-results resulting in incorrect reporting of test outcomes.",
      "recall_initiation_date": "20260429",
      "center_classification_date": "20260731",
      "report_date": "20260812",
      "code_info": "Software Version 2.5 UDI-DI code: 15099590802073",
      "more_code_info": ""
    }
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}