{
  "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",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "cfres_id": "114627",
      "product_res_number": "Z-0523-2013",
      "event_date_initiated": "2012-10-22",
      "event_date_posted": "2012-12-13",
      "recall_status": "Terminated",
      "event_date_terminated": "2013-01-24",
      "res_event_number": "63723",
      "product_code": "GRO",
      "product_description": "BD BBL Taxo XV Factor Strips, Catalog number 231104, in shelf pack vials, fifty strips/vial labeled in part ***Becton, Dickinson and Company, 7 Loveton Circle, Sparks, MD 21152 USA 800-638-8663, www.bd.com/ds***",
      "code_info": "Lot number 2089253",
      "firm_fei_number": "1119779",
      "recalling_firm": "Becton Dickinson & Co.",
      "address_1": "7 bd diagnostic systems loveton circle",
      "city": "Sparks",
      "state": "MD",
      "postal_code": "21152-0999",
      "additional_info_contact": "Ms. Gail Claiborne\n410-316-4054",
      "reason_for_recall": "In vitro diagnostic test kit was not manufactured according to specifications and may cause false negatives or misidentification of Hemophilus species present in patient specimens.",
      "root_cause_description": "Employee error",
      "action": "BD Diagnostic Systems sent an Urgent Product Recall letter dated October 22, 2012, to all affected customers..  The letter identified the product, the problem, and the action to be taken by the customer. Customers were advised to discontinue distribution and discard affected inventory for credit.  . Customers were requested to return a response form by fax to 410-316-4258.  For questions customers were instructed to contact BD Customer Service Department at 1-800-638-8663.  For assistance with replacements, customers were instructed to call 1-800-675-0908.\nFor questions regarding this recall call 410-316-4258.",
      "product_quantity": "650 vials",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) to international customers in Belgium, India, Japan, South Korea, Thailand and Mexico",
      "openfda": {
        "device_name": "Antisera, Fluorescent, All Types, Hemophilus Spp.",
        "medical_specialty_description": "Microbiology",
        "regulation_number": "866.3300",
        "device_class": "2",
        "k_number": [
          "K834067",
          "K851271",
          "K802423",
          "K800493"
        ]
      }
    }
  ]
}