{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Munchen",
      "state": "N/A",
      "country": "Germany",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92484",
      "recalling_firm": "Beckman Coulter Biomedical GmbH",
      "address_1": "Sauerbruchstr. 50",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US: AL\tCA\tFL\tIL\tIN\tKY\tMI\tMN\tMO\tNE\tNJ\tNV\tNY\tOH\tPA\tSC\tTX\tWI\tWV  OUS: Australia, Belgium, Canada, China, Croatia, Czechia, Egypt, France, Germany, Greece, Hong Kong, Ireland, Israel, Italy, Kazakhstan, Korea, Kuwait, Malaysia, Netherlands, New Zealand, Poland, Saudi Arabia, Spain, Switzerland, United Kingdom,",
      "recall_number": "Z-2145-2023",
      "product_description": "Beckman Coulter DxA Automation System, DxA 5000 Fit, REF: B87352, IVD, 200240V, 16A, 50/60HZ,  RxOnly",
      "product_quantity": "15",
      "reason_for_recall": "A software defect in the DxA Automation System may cause tests to be run on patient samples in tube types not compatible with the requested test, leading to erroneous patient results",
      "recall_initiation_date": "20230602",
      "center_classification_date": "20230714",
      "report_date": "20230726",
      "code_info": "UDI-DI: (01)15099590707118, All DxA serial numbers",
      "more_code_info": ""
    }
  ]
}