{
  "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": "2026-08-22",
    "results": {
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      "cfres_id": "39928",
      "product_res_number": "Z-0614-05",
      "event_date_initiated": "2005-05-27",
      "event_date_posted": "2005-09-07",
      "recall_status": "Terminated",
      "event_date_terminated": "2006-09-21",
      "res_event_number": "32377",
      "product_code": "MDB",
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      "code_info": "All Models (Not available in the US)",
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      "recalling_firm": "BIOMERIEUX, INC.",
      "address_1": "100 Rodolphe St",
      "city": "Durham",
      "state": "NC",
      "postal_code": "27712-9402",
      "additional_info_contact": "John Cusack, Sr.\n919-620-2803",
      "reason_for_recall": "A Bac T/ALERT 3D system failed to detect a positive sample in a pediatric BAC T/ALERT PF bottle.",
      "root_cause_description": "Other",
      "action": "Consignees were notified by letter on May 27, 2005.",
      "product_quantity": "337 units",
      "distribution_pattern": "Nationwide, Argentina, Australia/N. Zealand, Austria, Belgium, Brazil, Canada, Chile, China, Colombia, Denmark, Finland, France, Germany, Greece, Hong Kong, India, Italy, Ivory Coast, Japan, Korea, Mexico, Netherlands, Norway, Poland, Portugal, Russia, Sweden, Switzerland, Turkey, UK",
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