{
  "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": "Brea",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "78611",
      "recalling_firm": "Beckman Coulter Inc.",
      "address_1": "250 S Kraemer Blvd",
      "address_2": "N/A",
      "postal_code": "92821-6232",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "CA, AR, HI, CA, OH, WA, MD, Canada, Japan",
      "recall_number": "Z-0236-2018",
      "product_description": "UniCel DxH800, Part Numbers:  629029 and B24802,  automated hematology analyzer",
      "product_quantity": "15 units",
      "reason_for_recall": "The shield for the Single-Tube Station on the DxH instrument may interfere with sample aspiration in the open vial position.",
      "recall_initiation_date": "20171103",
      "center_classification_date": "20171213",
      "termination_date": "20180619",
      "report_date": "20171220",
      "code_info": "Serial Numbers:    B24802:  AW10161, AW10154, AZ34449, AZ34447  629029:  AT40563, AT06096, AT06095, AT02044, AW05080, AW05072, AW05066, AT50679, AS49422, AS36312, AS23151"
    }
  ]
}