{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "San Diego",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "97566",
      "recalling_firm": "CareFusion 303, Inc.",
      "address_1": "10020 Pacific Mesa Blvd",
      "address_2": "N/A",
      "postal_code": "92121-4386",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the countries of Canada, United Arab Emirates, Australia.",
      "recall_number": "Z-0369-2026",
      "product_description": "Various models of  BD Pyxis Pro 7-Drawer Auxiliary, Reference numbers: 1149-00 and  1152-00",
      "product_quantity": "32 units",
      "reason_for_recall": "Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.",
      "recall_initiation_date": "20250930",
      "center_classification_date": "20251027",
      "report_date": "20251105",
      "code_info": "All Serial Numbers/Ref #/UDI: 1149-00 10885403517822 and  1152-00 10885403517839"
    }
  ]
}