{
  "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": "71835",
      "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": "Distributed US (nationwide) including Puerto Rico and U.S. Virgin Islands and the countries of Bermuda, Canada, Guatemala, Hong Kong, Mexico, Panama, Taiwan, and Trinidad-Tobago.",
      "recall_number": "Z-2480-2015",
      "product_description": "COULTER LH Series Diluent, Catalog No. 8547194, Product Labeling A40192-AD.  The diluent provides the ability to analyze portions of the diluted blood sample for different blood cell types, such as red blood cells and platelets.",
      "product_quantity": "409,042 units (339,545 units in US)",
      "reason_for_recall": "Beckman Coulter is recalling the LH 750 and LH780 Hematology Systems because the use of the diluent lots may eventually result in a compromised Hgb cuvette.",
      "recall_initiation_date": "20150722",
      "center_classification_date": "20150828",
      "termination_date": "20151218",
      "report_date": "20150909",
      "code_info": "Lot Numbers: 510376F-510657F, M405229-M503553."
    }
  ]
}