{
  "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": "2026-08-13",
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      "product_res_number": "Z-0380-06",
      "event_date_initiated": "2005-11-23",
      "event_date_posted": "2006-01-11",
      "recall_status": "Terminated",
      "event_date_terminated": "2012-01-26",
      "res_event_number": "34247",
      "product_code": "JJF",
      "product_description": "Cytomics FC500 with\nCXP Software",
      "code_info": "Part Numbers 629636 629637",
      "firm_fei_number": "2050012",
      "recalling_firm": "Beckman Coulter Inc",
      "address_1": "200 S Kraemer Blvd",
      "city": "Brea",
      "state": "CA",
      "postal_code": "92822-6208",
      "additional_info_contact": "Nora Zerounian\n714-961-3634",
      "reason_for_recall": "Under certain conditions an incorrect Tube ID (Barcode) can be displayed and printed on the Runtime Panel Report in CXP Cytometer Software Version 2.0",
      "root_cause_description": "Software change control",
      "action": "A Product Corrective Action letter will be mailed the week of Nov 28, 2005 to all FC500 wi CXP Software customers. Each user will be contacted initially and then once more (if needed) in order to determine the rate of response from the Response form provided.",
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