{
  "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",
    "results": {
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    {
      "cfres_id": "35876",
      "product_res_number": "Z-0311-05",
      "event_date_initiated": "2004-10-20",
      "event_date_posted": "2004-12-16",
      "recall_status": "Terminated",
      "event_date_terminated": "2005-02-01",
      "res_event_number": "30443",
      "product_code": "GSO",
      "product_description": "BD, Brucella melitensis Antigen",
      "code_info": "Catalogue #240943, Lot #3046337",
      "firm_fei_number": "1025402",
      "recalling_firm": "BD Diagnostic Systems",
      "address_1": "1475 Athens Hwy",
      "city": "Grayson",
      "state": "GA",
      "postal_code": "30017-1538",
      "additional_info_contact": "Gail M. Claiborne\n410-316-4054",
      "reason_for_recall": "Febrile Antigens and Control Antisera that were released prior to August 2003 contained the 12/2000 revised insert that had incorrect testing instructions.",
      "root_cause_description": "Other",
      "action": "Consignees were notified by letter beginning 10/20/2004.",
      "product_quantity": "120 vials (5 ml per vial)",
      "distribution_pattern": "Nationwide, Australia, Belgium, Canada, Chile, Ecuador, India, Korea, Malaysia, New Zealand, Singapore, Taiwan",
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          "3024463179",
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        "device_name": "Antigens (Febrile), Agglutination, Brucella Spp.",
        "medical_specialty_description": "Microbiology",
        "regulation_number": "866.3085",
        "device_class": "2"
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}