{
  "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": "Ongoing",
      "city": "Brea",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83732",
      "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": "US: NY, VA    OUS:  Austria Belgium Czech Republic  France Germany Israel  Italy Lithuania Mayotte  Romania Slovakia South Africa  Spain Sweden Switzerland  United Kingdom",
      "recall_number": "Z-0492-2020",
      "product_description": "AutoMate 1250, Sorter with Aliquot Module - UDI: 15099590364106; Model #ODL25125   Automate 2550, High Speed Sorter with Aliquot Module - UDI: 15099590364083 , Model #ODL25255",
      "product_quantity": "83 automate systems",
      "reason_for_recall": "Beckman Coulter has identified a case where a customer using the microltiterplate kit option without a sorting drive encountered a cross-contamination of samples when a connection time-out occurred between the system and Laboratory Information System (LIS) .",
      "recall_initiation_date": "20181109",
      "center_classification_date": "20191118",
      "report_date": "20191127",
      "code_info": "All units containing software Version(s) 4.1.1 and up"
    }
  ]
}