{
  "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": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "cfres_id": "216046",
      "product_res_number": "Z-0369-2026",
      "event_date_initiated": "2025-09-30",
      "event_date_posted": "2025-10-27",
      "recall_status": "Open, Classified",
      "res_event_number": "97566",
      "product_code": "BRY",
      "product_description": "Various models of  BD Pyxis Pro 7-Drawer Auxiliary, Reference numbers: 1149-00 and\n1152-00",
      "code_info": "All Serial Numbers/Ref #/UDI: 1149-00\t10885403517822 and \n1152-00\t10885403517839",
      "firm_fei_number": "2016493",
      "recalling_firm": "CareFusion 303, Inc.",
      "address_1": "10020 Pacific Mesa Blvd",
      "city": "San Diego",
      "state": "CA",
      "postal_code": "92121-4386",
      "additional_info_contact": "BD Technical Support\n1800-727-6102",
      "reason_for_recall": "Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.",
      "root_cause_description": "Under Investigation by firm",
      "action": "On September 30, 2025, BD issue a Urgent Medical Device Recall Expansion notification to affected consignees via FedEx. BD is asking consignees to take the following actions: \n\n1. Affected products can continue to be used per existing Manuals and Guides.\n2. In the event of an accidental fluid spill on the device or in a drawer, users should following instructions outlined within the customer notification. \n3. Review the customer letter attachment  which provides warnings, cautions and recommendations regarding fluid ingress. \n4. Complete the attached Customer Response Form and return to the BD contact noted on the form whether or not you have any of the impacted material.",
      "product_quantity": "32 units",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the countries of Canada, United Arab Emirates, Australia.",
      "openfda": {
        "device_name": "Cabinet, Table And Tray, Anesthesia",
        "medical_specialty_description": "Anesthesiology",
        "regulation_number": "868.6100",
        "device_class": "1",
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