{
  "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": "2026-08-20",
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      "recall_status": "Terminated",
      "event_date_terminated": "2016-05-27",
      "res_event_number": "72548",
      "product_code": "MVU",
      "product_description": "BD CD64 APC-R700;\nAnalyte Specific Reagent; Model 657701; Lot No. 4344945, 5037611 and 5063945.\n\nHematology - used as analyte specific reagent  - contamination leads to possibility of unexpected staining pattern.",
      "code_info": "Model 657701; Lot No. 4344945, 5037611, both with expiry date of 31 DEC 2015; and 5063945 with expiry dte of 29 FEB 2016.",
      "firm_fei_number": "2916837",
      "recalling_firm": "Becton, Dickinson and Company, BD Biosciences",
      "address_1": "2350 Qume Dr",
      "city": "San Jose",
      "state": "CA",
      "postal_code": "95131-1812",
      "additional_info_contact": "Melissa J. Quinn\n408-954-6080",
      "reason_for_recall": "Three lots of CD64 (MD22) are contaminated with CD4 antibody.",
      "root_cause_description": "Process control",
      "action": "Urgent Product Recall letters were sent out on October 30, 2015 via certified mail to notify customers of the issue.",
      "product_quantity": "23 vials",
      "distribution_pattern": "Distributed in the states of FL, WA, PA, IL, GA, RI, TX, ND, and IA.",
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